(237 days)
Not Found
No
The description focuses on the hardware and basic control mechanisms of an IPL device. There is no mention of algorithms, data processing for decision making, or any features that suggest learning or intelligent analysis of data.
Yes
The device is described as a "Phototherapy unit (model: 10PL)" and its "Intended Use" states it is for treating various "conditions" such as Melasma, Rosacea, and Port wine stains using filtered Intense Pulsed Light. Treating conditions to alleviate or cure them is a therapeutic application.
No
The device is an IPL phototherapy unit intended for therapeutic treatment of skin conditions, not for diagnosis.
No
The device description clearly details hardware components such as a power supply, SMPS, capacitor, xenon lamp, handpiece, motor pump, cooling fan, and a touch screen operation panel. It is a physical device that uses Intense Pulsed Light.
Based on the provided information, this device is not an IVD (In Vitro Diagnostic).
Here's why:
- Intended Use: The intended use is for "surgical and aesthetic applications in dermatology" using Intense Pulsed Light to treat skin conditions. This involves applying light energy directly to the patient's skin for therapeutic purposes.
- Device Description: The description details a system that generates and delivers pulsed light to the skin. It focuses on the technical aspects of light generation, filtering, and delivery.
- Lack of In Vitro Activity: An IVD is a medical device intended to be used in vitro for the examination of specimens derived from the human body in order to provide information for diagnostic, monitoring or compatibility purposes. This device does not involve the examination of specimens outside of the body.
The device is a therapeutic device that uses light energy to treat conditions directly on the patient's skin. This falls under the category of a medical device, but not specifically an In Vitro Diagnostic device.
N/A
Intended Use / Indications for Use
The Photo therapy unit (model: 10PL) is intended for use in surgical and aesthetic applications in dermatology by using filtered Intense Pulsed Light to treat the following conditions with different wavelengths to skin types I-IV.
| Wavelengths | Conditions |
|---|---|
| 415nm - 950nm | Melasma |
| 570nm - 950nm | Melasma, Rosacea |
| 590nm - 950nm | Rosacea, Port wine stains |
Product codes (comma separated list FDA assigned to the subject device)
ONF
Device Description
When the key switch is turned on for the first time [ON], the power supply to remove noise by receiving general power (AC120V) from the block diagram is applied to the SMPS to obtain the power supply and DC12V, the power used for the motor pump and cooling fan and the main control board.
POWER SUPPLY is a device that charges DC high voltage using SMPS by receiving stable power, and generates maximum DC600V±10% to charge the CAPACITOR.
When the charged DC voltage is applied to the xenon lamp of the handpiece, a desired wavelength is selected among the emitted rays, and the push button switch is pressed the rays are irradiated.
In order to use the light irradiator safely, a motor pump and a cooling fan are used to circulate the coolant to cool the xenon lamp and operate the thermoelectric module in the handpiece to keep the folter set to the desired temperature.
Set the output intensity and operation mode on the touch screen operation panel of the LCD monitor of the main control board, and select the READY button to turn on the xenon lamp, and press the push button switch to irradiate the light.
10PL is IPL device of Tentech Co., Ltd. that has technical advantages which adopted the rotary filter which can change wavelength band by rotating a revolver without replacing handpieces or filters unlike the existing IPL (Intense Pulsed Light)
Mentions image processing
Not Found
Mentions AI, DNN, or ML
Not Found
Input Imaging Modality
Not Found
Anatomical Site
Skin (in dermatology)
Indicated Patient Age Range
Not Found
Intended User / Care Setting
Surgical and aesthetic applications in dermatology. This implies use by trained professionals in a clinical setting.
Description of the training set, sample size, data source, and annotation protocol
Not Found
Description of the test set, sample size, data source, and annotation protocol
Not Found
Summary of Performance Studies (study type, sample size, AUC, MRMC, standalone performance, key results)
No clinical studies were considered necessary and performed.
Bench tests were conducted to verify that the proposed device met all design specifications. The test results demonstrated that the proposed device complies with the following standards:
- AASI AAMI ES60601-1:2005/(R)2012 and A1:2012
- IEC 60601-1-6:2010/A1:2013
- IEC 60601-2-57:2011
- IEC 60601-1-2:2014
- IEC 62471:2006
Software validation: The 10PL contains MODERATE level of concern software. Software was designed and developed according to a software development process and was verified and validated.
Biocompatibility: The part of 10PL in contact with the patient was verified and demonstrated for the safety of materials through the biocompatibility test in accordance with ISO 10993-1.
- Cytotoxicity test according to ISO 10993-5
- Intracutaneous (intradermal) reactivity test according to ISO 10993-10
- Skin sensitization test according to ISO 10993-10
Key Metrics (Sensitivity, Specificity, PPV, NPV, etc.)
Not Found
Predicate Device(s): If the device was cleared using the 510(k) pathway, identify the Predicate Device(s) K/DEN number used to claim substantial equivalence and list them here in a comma separated list exactly as they appear in the text. List the primary predicate first in the list.
Reference Device(s): Identify the Reference Device(s) K/DEN number and list them here in a comma separated list exactly as they appear in the text.
Not Found
Predetermined Change Control Plan (PCCP) - All Relevant Information for the subject device only (e.g. presence / absence, what scope was granted / cleared under the PCCP, any restrictions, etc).
Not Found
§ 878.4810 Laser surgical instrument for use in general and plastic surgery and in dermatology.
(a)
Identification. (1) A carbon dioxide laser for use in general surgery and in dermatology is a laser device intended to cut, destroy, or remove tissue by light energy emitted by carbon dioxide.(2) An argon laser for use in dermatology is a laser device intended to destroy or coagulate tissue by light energy emitted by argon.
(b)
Classification. (1) Class II.(2) Class I for special laser gas mixtures used as a lasing medium for this class of lasers. The devices subject to this paragraph (b)(2) are exempt from the premarket notification procedures in subpart E of part 807 of this chapter, subject to the limitations in § 878.9.
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Image /page/0/Picture/0 description: The image contains two logos. On the left is the Department of Health & Human Services logo. On the right is the FDA logo, which includes the letters "FDA" in a blue square, followed by the words "U.S. FOOD & DRUG ADMINISTRATION" in blue text.
November 10, 2022
Tentech Co. Ltd. Lee Dong Gun Quality Assurance Manager 3F Hyungkyung Building, 611, Seolleung-ro Gangnam-gu, Seoul 06103 Korea. South
Re: K220794
Trade/Device Name: 10PL Regulation Number: 21 CFR 878.4810 Regulation Name: Laser Surgical Instrument For Use In General And Plastic Surgery And In Dermatology Regulatory Class: Class II Product Code: ONF Dated: September 29, 2022 Received: October 11, 2022
Dear Lee Dong Gun:
We have reviewed your Section 510(k) premarket notification of intent to market the device referenced above and have determined the device is substantially equivalent (for the indications for use stated in the enclosure) to legally marketed predicate devices marketed in interstate commerce prior to May 28, 1976, the enactment date of the Medical Device Amendments, or to devices that have been reclassified in accordance with the provisions of the Federal Food, Drug, and Cosmetic Act (Act) that do not require approval of a premarket approval application (PMA). You may, therefore, market the device, subject to the general controls provisions of the Act. Although this letter refers to your product as a device, please be aware that some cleared products may instead be combination products. The 510(k) Premarket Notification Database located at https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm identifies combination product submissions. The general controls provisions of the Act include requirements for annual registration, listing of devices, good manufacturing practice, labeling, and prohibitions against misbranding and adulteration. Please note: CDRH does not evaluate information related to contract liability warranties. We remind you, however, that device labeling must be truthful and not misleading.
If your device is classified (see above) into either class II (Special Controls) or class III (PMA), it may be subject to additional controls. Existing major regulations affecting your device can be found in the Code of Federal Regulations, Title 21, Parts 800 to 898. In addition, FDA may publish further announcements concerning your device in the Federal Register.
Please be advised that FDA's issuance of a substantial equivalence determination does not mean that FDA has made a determination that your device complies with other requirements of the Act or any Federal
1
statutes and regulations administered by other Federal agencies. You must comply with all the Act's requirements, including, but not limited to: registration and listing (21 CFR Part 807); labeling (21 CFR Part 801); medical device reporting of medical device-related adverse events) (21 CFR 803) for devices or postmarketing safety reporting (21 CFR 4, Subpart B) for combination products (see https://www.fda.gov/combination-products/guidance-regulatory-information/postmarketing-safety-reportingcombination-products); good manufacturing practice requirements as set forth in the quality systems (QS) regulation (21 CFR Part 820) for devices or current good manufacturing practices (21 CFR 4, Subpart A) for combination products; and, if applicable, the electronic product radiation control provisions (Sections 531-542 of the Act); 21 CFR 1000-1050.
Also, please note the regulation entitled, "Misbranding by reference to premarket notification" (21 CFR Part 807.97). For questions regarding the reporting of adverse events under the MDR regulation (21 CFR Part 803), please go to https://www.fda.gov/medical-device-safety/medical-device-reportingmdr-how-report-medical-device-problems.
For comprehensive regulatory information about medical devices and radiation-emitting products, including information about labeling regulations, please see Device Advice (https://www.fda.gov/medicaldevices/device-advice-comprehensive-regulatory-assistance) and CDRH Learn (https://www.fda.gov/training-and-continuing-education/cdrh-learn). Additionally, you may contact the Division of Industry and Consumer Education (DICE) to ask a question about a specific regulatory topic. See the DICE website (https://www.fda.gov/medical-device-advice-comprehensive-regulatoryassistance/contact-us-division-industry-and-consumer-education-dice) for more information or contact DICE by email (DICE@fda.hhs.gov) or phone (1-800-638-2041 or 301-796-7100).
Sincerely,
Image /page/1/Picture/5 description: The image shows the name "Jianting Wang -S" in a large, sans-serif font. The text is black and appears to be centered on a white background. The name is written in a clear and legible manner, with a hyphen separating the last name from the letter 'S'.
Jianting Wang Acting Assistant Director DHT4A: Division of General Surgery Devices OHT4: Office of Surgical and Infection Control Devices Office of Product Evaluation and Ouality Center for Devices and Radiological Health
Enclosure
2
Indications for Use
510(k) Number (if known) K220794
Device Name 10PL
Indications for Use (Describe)
The Photo therapy unit (model: 10PL) is intended for use in surgical and aesthetic applications in dermatology by using filtered Intense Pulsed Light to treat the following conditions with different wavelengths to skin types I-IV.
| Wavelengths | Conditions |
|---|---|
| 415nm - 950nm | Melasma |
| 570nm - 950nm | Melasma, Rosacea |
| 590nm - 950nm | Rosacea, Port wine stains |
| Type of Use (Select one or both, as applicable) | |
|---|---|
| ☑ Prescription Use (Part 21 CFR 801 Subpart D) | ☐ Over-The-Counter Use (21 CFR 801 Subpart C) |
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Image /page/3/Picture/0 description: The image shows the logo for TEN TECH. The logo is in blue and black, with the word "TEN" in blue and the word "TECH" in black. There is a gray swoosh under the logo. The logo is simple and modern.
510(k) Summary K220794
[As required by 21 CFR 807.92]
Date Prepared [21 CFR 807.92(a)(a)] 1.
November 08, 2022
Submitter's Information & Contact Person [21 CFR 807.92(a)(1)] 2.
-
Name of Manufacturer: Tentech Co., Ltd.
-
Address: 3F, Hyunkyung Building, 611, Seolleung-ro, Gangnam-gu, Seoul, 06103, Republic of Korea
-
Contact Name: Dong Gun, Lee
-
Telephone No.: 82-(0)2-6954-2203
-
Fax No.: 82-(0)2-3444-4999
-
Email Address: tentech.rnd@@gmail.com
Trade Name, Common Name, Classification [21 CFR 807.92(a)(2)] 3.
Common name: Photo therapy unit Trade name: 10PL
| Classification Description | 21 CFR Section | Product Code |
|---|---|---|
| Powered Light based Non-Laser Surgical Instrument | ||
| With Thermal Effect | 878.4810 | ONF |
As stated in 21 CFR, parts 878.4810, this generic types of devices has been classified as Class II.
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4. Identification of Predicate Device(s) [21 CFR 807.92(a)(3)[
The identified predicate devices within this submission are shown as follow:
Predicate device 1
| • 510(k) Number: | K102857 |
|---|---|
| • Applicant: | Ahwon Medi Instrument. |
| • Classification Name: | Laser surgical instrument for use in general and plastic surgery and in dermatology |
| • Trade Name: | R2PL System |
Predicate device 2
| ● | 510(k) Number: | K181868 |
|---|---|---|
| ● | Applicant: | IDS, Ltd. |
| ● | Classification Name: | Laser surgical instrument for use in general and plastic surgery and |
| in dermatology | ||
| ● | Trade Name: | SHINY RPL System |
Predicate device 3
| • 510(k) Number: | K192539 |
|---|---|
| • Applicant: | El. EN. Electronic Engineering SPA |
| • Classification Name: | Laser surgical instrument for use in general and plastic surgery and |
| in dermatology | |
| • Trade Name: | Deka Luxea “LAZUR Pulsed Light handpiece” |
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Image /page/5/Picture/0 description: The image shows the logo for TenTech. The word "TEN" is in blue, and the word "TECH" is in black. There is a swoosh design that goes from under the "T" in "TEN" to the "T" in "TECH".
Description of the Device [21 CFR 807.92(a)(4)] 5.
When the key switch is turned on for the first time [ON], the power supply to remove noise by receiving general power (AC120V) from the block diagram is applied to the SMPS to obtain the power supply and DC12V, the power used for the motor pump and cooling fan and the main control board.
POWER SUPPLY is a device that charges DC high voltage using SMPS by receiving stable power, and generates maximum DC600V±10% to charge the CAPACITOR.
When the charged DC voltage is applied to the xenon lamp of the handpiece, a desired wavelength is selected among the emitted rays, and the push button switch is pressed the rays are irradiated.
In order to use the light irradiator safely, a motor pump and a cooling fan are used to circulate the coolant to cool the xenon lamp and operate the thermoelectric module in the handpiece to keep the folter set to the desired temperature.
Set the output intensity and operation mode on the touch screen operation panel of the LCD monitor of the main control board, and select the READY button to turn on the xenon lamp, and press the push button switch to irradiate the light.
10PL is IPL device of Tentech Co., Ltd. that has technical advantages which adopted the rotary filter which can change wavelength band by rotating a revolver without replacing handpieces or filters unlike the existing IPL (Intense Pulsed Light)
Indications for Use [21 CFR 807.92(a)(5)] 6.
The Photo therapy unit (model: 10PL) is intended for use in surgical and aesthetic applications in dermatology
by using filtered Intense Pulsed Light to treat the following conditions with different wavelengths to skin types I-IV.
| Wavelengths | Conditions |
|---|---|
| 415 - 950nm | Melasma |
| 570 - 950nm | Melasma, Rosacea |
| 590 - 950nm | Rosacea, Port wine stains |
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Image /page/6/Picture/0 description: The image shows the logo for TEN TECH. The logo is in blue and black, with the word "TEN" in blue and the word "TECH" in black. There is a gray swoosh under the word "TEN". The logo is simple and modern.
7. Determination of Substantial Equivalence [21 CFR 807.92(a)(6) and 21 CFR 807.92(b)]
There are no significant differences between the 10PL and the predicate devices that would adversely affect the use of the product. It is substantially equivalent to this device in design, function, and technical characteristics.
| Proposed Device | Predicate Device #1 | Predicate Device #2 | SE decision | |||||||||||||||||||||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| K Number | K220794 | K102857 | K181868 | - | ||||||||||||||||||||||||||||||||||
| Manufacturer | Tentech Co., Ltd. | Ahwon medi Instrument. | IDS, Ltd. | - | ||||||||||||||||||||||||||||||||||
| Trade Name | Photo therapy unit | R2PLTM System | SHINY RPL System | - | ||||||||||||||||||||||||||||||||||
| Indications for Use | The Photo therapy unit (model: 10PL) is intended for use in surgical and aesthetic applications in dermatology by using filtered Intense Pulsed Light to treat the following conditions with different wavelengths to skin types I-IV. | |||||||||||||||||||||||||||||||||||||
| Wavelength Condition 415-950 nm Melasma 570-950 nm Melasma, Rosacea 590-950 nm Rosacea, Port wine stains | The Ahwon R2PL system intended use for in Surgical, Asthetic and Cosmetic Application in Dermatology by using filtered Intense Pulsed Light to treat the following conditions with different wavelengths to skin types I-IV. | |||||||||||||||||||||||||||||||||||||
| Wavelength Condition 415-950 nm Acne, Vulgaris 560-950 nm Melasma, Ephelides 590-950 nm Port wine stains, Rosacea 640-1200nm Melasma 695-1200nm Hair reduction.Re moval Vascular lesions | The IDS SHINY IPL system is intended for use in Surgical, Aesthetic and Cosmetic applications in Dermatology by by using filtered Intense Pulsed Light to treat the following conditions with different wavelengths to skin types I-IV. | |||||||||||||||||||||||||||||||||||||
| Wavelength Condition 415-950 nm Acne, Vulgaris 560-950 nm Melasma, Ephelides 640-950 nm Acne, Hair Reduction 640-1200nm Hair Reduction 695-1200nm Hair Reduction 755-1200nm Hair Reduction | - | |||||||||||||||||||||||||||||||||||||
| Energy Density | 5-35J/cm2 | 5-40J/cm2 | 5-40J/cm2 | Different |
Table 1. General Comparison of Photo therapy unit
Different - Energy Density
The Energy density for proposed device is different from the predicate devices. However, the Energy Density of the proposed Photo therapy unit is covered by the range of the Energy Density of the predicate device. Therefore, this difference does not affect substantially equivalence on safety and effectiveness
| Wavelength | 415-950 nm
570-950 nm
590-950 nm | 415nm – 950nm
560nm – 950nm
590nm – 1200nm
640nm – 1200nm
695nm – 1200nm | 415nm – 950nm
560nm – 950nm
640nm – 950nm
640nm – 1200nm
695nm – 1200nm
725nm – 1200nm | Different |
| ------------ | ---------------------------------------- | -------------------------------------------------------------------------------------- | ------------------------------------------------------------------------------------------------------- | ----------- |
|---|
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Image /page/7/Picture/0 description: The image shows the logo for TEN TECH. The word "TEN" is in blue, and the word "TECH" is in black. There is a gray swoosh under the words. The logo is simple and modern.
3F, Hyunkyung Building, 611, Seolleung-ro, Gangnam-gu, Seoul, 06103, Republic of Korea
TEL: +82 02 6954 2203 FAX: +82 02 3444 4999
| Proposed Device | Predicate Device #1 | Predicate Device #2 | SE decision | |
|---|---|---|---|---|
| Different - Wavelength | ||||
| The Wavelength for proposed device is different from the predicate devices. However, the Wavelength of the proposed Photo | ||||
| therapy unit is covered by the range of the Wavelength of the predicate device. Therefore, this difference does not affect | ||||
| substantially equivalence on safety and effectiveness | ||||
| The 415-950 nm was compared with the predicate device in the LAZUR Pulsed Light handpiece in Table 2. | ||||
| Pulse width | 2.0-35.0ms(On Time) | |||
| 3.0-60.0ms(Off Time) | SE | |||
| Laser Delivery | ||||
| Type | Articulated Arm with Handpiece | SE | ||
| Light Transfer | ||||
| Method | Handpiece revolver | SE |
Table 2. General Comparison of Indication for use
| Proposed Device | Predicate Device #3 | SE decision | |
|---|---|---|---|
| K Number | K220794 | K192539 | - |
| Manufacturer | Tentech Co., Ltd. | El. EN. Electronic Engineering SPA | - |
| Trade Name | Photo therapy unit | Deka Luxea | |
| "LAZUR Pulsed Light handpiece" | - | ||
| Indications for | |||
| Use | The Photo therapy unit (model: 10PL) is | ||
| intended for use in surgical and aesthetic | |||
| applications in dermatology by using | |||
| filtered Intense Pulsed Light to treat the | |||
| following conditions with different | |||
| wavelengths to skin types I-IV. |
Wavelength
415-950 nm
570-950 nm
590-950 nm | LAZUR Pulsed Light handpiece:
The handpiece (with and without contact-
cooling) is indicated for:
- The treatment of benign pigmented
epidermal lesions including dyschromia,
hyperpigmentation, melasma, and ephelides
(freckles). | |
| | Condition
Melasma
Melasma, Rosacea
Rosacea, Port wine stains | | |
| Wavelength | 415-950 nm | 420-950nm | SE |
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Image /page/8/Picture/0 description: The image shows the logo for TEN TECH. The word "TEN" is in blue, and the word "TECH" is in black. The logo has a curved line underneath the word "TEN".
Non-Clinical Test Summary [21 CFR 807.92(b)(1)] 8.
1) Electrical Safety, Electromagnetic Compatibility Testing
Bench tests were conducted to verify that the proposed device met all design specifications. The test results demonstrated that the proposed device complies with the following standards:
| Standard
| (Edition) | Standard Title |
|---|---|
| AASI AAMI ES60601-1:2005/(R)2012 and A1:2012 | Medical electrical equipment – Part 1: General requirements for basic safety and essential performance |
| IEC 60601-1-6:2010/A1:2013 | Medical electrical equipment - Part 1-6: General requirements for safety - Collateral standard: Usability |
| IEC 60601-2-57:2011 | Medical electrical equipment – Part 2: Particular requirements for the basic safety and essential performance of non-laser light source equipment intended for therapeutic, diagnostic, monitoring and cosmetic/aesthetic use |
| IEC 60601-1-2:2014 | Medical electrical equipment - Part 1-2: General requirements for basic safety and essential performance – Collateral standard: Electromagnetic compatibility – Requirements and tests |
| IEC 62471:2006 | Photobiological safety of lamps and lamp systems. |
2) Software Validation
The 10PL contains MODERATE level of concern software. Software was designed and developed according to a software development process and was verified and validated.
The software information is provided in accordance with FDA guidance: The content of premarket submissions for software contained in medical devices, on November 4, 2021.
3) Biocompatibility
The part of 10PL in contact with the patient was verified and demonstrated for the safety of materials through the biocompatibility test in accordance with ISO 10993-1.
- -Cytotoxicity test according to ISO 10993-5
- Intracutaneous (intradermal) reactivity test according to ISO 10993-10 -
- Skin sensitization test according to ISO 10993-10 -
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Image /page/9/Picture/0 description: The image shows the logo for TEN TECH. The logo is in blue and black. The word "TEN" is in blue and the word "TECH" is in black.
9. Clinical Test Summary [21 CFR 807.92(b)(2)]
No clinical studies were considered necessary and performed.
10. Conclusion [21 CFR 807.92(b)(3)]
In according with the Federal Food & drug and cosmetic Act, 21 CFR Part 807, and based on the information provided in this premarket notification Tentech Co,. Ltd. concludes that the 10PL is substantially equivalent to predicate devices as described herein.