Predicate Devices

Reference Devices

Not Found

AI/ML (Artificial Intelligence / Machine Learning)

No
The description focuses on the device's IPL technology and standard electrical/biological safety testing. There is no mention of AI, ML, image processing, or data sets typically associated with AI/ML development.

Therapeutic

Yes
The device is indicated for permanent hair reduction, which is a therapeutic effect. It works by heating the hair root to reduce hair growth.

Diagnostic

No

This device is for hair removal and permanent hair reduction using Intense Pulsed Light (IPL). Its intended use is treatment, not diagnosis of any condition.

SaMD (Software as a Medical Device)

No

The device description explicitly states it is an "IPL DEVICE" and includes physical components like a power supply and has specified weight and dimensions. It also mentions electrical safety and electromagnetic compatibility testing, which are relevant to hardware. While software verification and validation are mentioned, this is for software contained in the medical device, not a standalone software-only device.

IVD (In Vitro Diagnostic)

No, this device is not an IVD (In Vitro Diagnostic).

Here's why:

IVD Definition: In Vitro Diagnostics are medical devices used to examine specimens taken from the human body (like blood, urine, or tissue) to provide information for diagnosis, monitoring, or screening.
Device Function: The IPL Hair Remover Device works by applying Intense Pulsed Light directly to the skin to target hair follicles. It does not analyze any biological specimens taken from the body.
Intended Use: The intended use is for the removal and permanent reduction of unwanted hair, which is a cosmetic or aesthetic procedure, not a diagnostic one.

The information provided clearly describes a device that interacts directly with the body's surface for a non-diagnostic purpose.

PCCP (Predetermined Change Control Plan) Authorized

N/A

Overview

# Intended Use / Indications for Use
The IPL Hair Remover Device, Model: G993, G996, G998 and G885 is indicated for the removal of unwanted hair under the direction of a physician, after training by a healthcare professional. The device is also indicated for the permanent reduction in hair regrowth, defined as the long-term, stable reduction in the number of hairs re-growing when measured at 6, 9 and 12 months after the completion of a treatment regime. The device is used for adults.

# Product codes
ONF

# Device Description
IPL Hair Remover, Model: G993, G996, G998 and G885 is a small prescription-use device for the permanent reduction of hair growth based on Intense Pulsed Light (IPL). It works below the skin's surface and does not involve any cutting or pulling, reducing hair growth with minimal pain. It is a personal Light-Based Hair Removal System. Permanent hair reduction is defined as the long-term stable reduction in the number of hairs re-growing when measured at 6, 9 and 12 months after the completion of a treatment regimen. Emission is by finger switch. Device includes IPL DEVICE. Power supply and User manual. It is used AC Powered (100-240 V AC). The weight of the device is 215.1g, and the size is 188 x 76 x 49mm (H*W*D). The device incorporates Intense Pulse Light (IPL) technology. The purpose of the light is to heat the root where the hair grows.

# Mentions image processing
Not Found

# Mentions AI, DNN, or ML
Not Found

# Input Imaging Modality
Intense Pulsed Light

# Anatomical Site
Not Found

# Indicated Patient Age Range
adults

# Intended User / Care Setting
under the direction of a physician, after training by a healthcare professional.

# 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)
IPL Hair Remover, Model: G993, G996, G998 and G885 has been evaluated the safety and performance by lab bench testing as following:
- Electrical safety test according to IEC 60601-1, IEC60601-1-11 and IEC 60601-2-57 standards
- Electromagnetic compatibility test according to IEC 60601-1-2 standard
- ISO 10993-5:2009/(R) 2014, Biological Evaluation of Medical Devices -- Part 5: Tests For In Vitro Cytotoxicity.
- ISO 10993-10:2010, Biological Evaluation of Medical Devices - Part 10: Tests for Irritation and Skin Sensitization.
- Software verification and validation test according to the requirements of the FDA "Guidance for PreMarket Submissions and for Software Contained in Medical Devices"
Clinical testing: No clinical trial is necessary in the submission.

# Key Metrics (Sensitivity, Specificity, PPV, NPV, etc.)
Not Found

# Predicate Device(s)
[K160968](https://510k.innolitics.com/search/K160968), [K172791](https://510k.innolitics.com/search/K172791), [K190820](https://510k.innolitics.com/search/K190820)

# Reference Device(s)
Not Found

# Predetermined Change Control Plan (PCCP) - All Relevant Information
Not Found

Regulation Number and Section

§ 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.

Summary

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Image /page/0/Picture/0 description: The image contains the logo of the U.S. Food and Drug Administration (FDA). The FDA logo consists of two parts: the Department of Health and Human Services logo on the left and the FDA acronym along with the full name of the agency on the right. The Department of Health and Human Services logo is a stylized human figure, while the FDA part includes the acronym "FDA" in a blue square, followed by "U.S. FOOD & DRUG ADMINISTRATION" in blue text.

October 4, 2021

Shenzhen Mywin Technology Co., Ltd. % Jet Li Regulation Manager Guangzhou KEDA Biological Tech Co., Ltd. 6F, No.1 TianTai road, Science City, LuoGang District GuangZhou, Guangdong China

Re: K211368

Trade/Device Name: IPL Hair Remover, Model: G993, G996, G998 and G885 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 3, 2021 Received: September 13, 2021

Dear Jet Li:

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.

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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 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 and Part 809); 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 mediation-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,

Purva U. Pandya -S

Purva Pandya 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

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Indications for Use

510(k) Number (if known) K211368

Device Name

IPL Hair Remover, Model: G993, G996, G998 and G885

Indications for Use (Describe)

The IPL Hair Remover Device, Model: G993, G996, G998 and G885 is indicated for the removal of unwanted hair under the direction of a physician, after training by a healthcare professional. The device is also indicated for the permanent reduction in hair regrowth, defined as the long-term, stable reduction in the number of hairs re-growing when measured at 6, 9 and 12 months after the completion of a treatment regime. The device is used for adults.

Type of Use (Select one or both, as applicable)
X Prescription Use (Part 21 CFR 801 Subpart D)	Over-The-Counter Use (21 CFR 801 Subpart C)

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Date of the summary prepared: June 11, 2021

510(k) Summary

This summary of 510(K) safety and effectiveness information is being submitted in accordance with the requirement of 21 CFR 807.92.

1. Submitter's Information

Sponsor

Company Name: Shenzhen Mywin Technology Co., Ltd. �
Address: 2nd Floor, Building B, New Age gongrong Industrial Zone, No. 2, Shihuan Road, � Shilong community, Shiyan Street, Baoan District, Shenzhen 518103,China
Phone: +86-18902842323 �
� Contact Person: Meiyun Liu
E-mail: Szmywin@163.com �

Application Correspondent:

� Guangzhou KEDA Biological Tech Co., Ltd.
� Address: 6F, No.1 TianTai road, Science City, LuoGang District, GuangZhou City, China
Contact Person: Mr. Jet Li �
� Tel: +86-18588874857
� Email: Med-jl@foxmail.com

2. Subject Device Information

� Trade Name: IPL Hair Remover, Model: G993, G996, G998 and G885
- Powered Light Based Non-Laser Surgical Instrument With Common Name:
� Thermal Effect
Laser Surgical Instrument For Use In General And Plastic � Classification name: Surgery And In Dermatology
General & Plastic Surgery Review Panel: �
ONF � Product Code:
� Regulation Class: 2
878.4810 � Regulation Number:

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| Sponsor | CyDen Limited. | Conair Corporation | Kam Yuen Plastic
Products Ltd. |
|----------------------|-------------------------------|---------------------------------------------|-----------------------------------|
| Device Name | Ipulse
Gold Hair
Device | Smoothskin
Lumilisse IPL Hair
Remover | Aimanfun
Comfort
Lumea |
| 510(k)
Number | K160968 | K172791 | K190820 |
| Regulation
Number | 878.4810 | 878.4810 | 878.4810 |
| Regulation Class | 2 | 2 | 2 |

3. Predicate Device Information

4. Device Description

IPL Hair Remover, Model: G993, G996, G998 and G885 is a small prescription-use device for the permanent reduction of hair growth based on Intense Pulsed Light (IPL). It works below the skin's surface and does not involve any cutting or pulling, reducing hair growth with minimal pain. It is a personal Light-Based Hair Removal System. Permanent hair reduction is defined as the longterm stable reduction in the number of hairs re-growing when measured at 6, 9 and 12 months after the completion of a treatment regimen. Emission is by finger switch. Device includes IPL DEVICE. Power supply and User manual. It is used AC Powered (100-240 V AC). The weight of the device is 215.1g, and the size is 188 x 76 x 49mm (HWD). The device incorporates Intense Pulse Light (IPL) technology. The purpose of the light is to heat the root where the hair grows.

5. Indications for Use

The IPL Hair Remover Device (Model: G993, G996, G998 and G885) is indicated for the removal of unwanted hair under the direction of a physician, after training by a healthcare professional. The device is also indicated for the permanent reduction in hair regrowth, defined as the longterm, stable reduction in the number of hairs re-growing when measured at 6, 9 and 12 months after the completion of a treatment regime. The device is used for adults.

6. Test Summary

IPL Hair Remover, Model: G993, G996, G998 and G885 has been evaluated the safety and

performance by lab bench testing as following:

� Electrical safety test according to IEC 60601-1, IEC60601-1-11 and IEC 60601-2-57 standards
� Electromagnetic compatibility test according to IEC 60601-1-2 standard
� ISO 10993-5:2009/(R) 2014, Biological Evaluation of Medical Devices -- Part 5: Tests For In Vitro Cytotoxicity.
� ISO 10993-10:2010, Biological Evaluation of Medical Devices - Part 10: Tests for Irritation and Skin Sensitization.

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� Software verification and validation test according to the requirements of the FDA "Guidance for PreMarket Submissions and for Software Contained in Medical Devices"
Clinical testing: No clinical trial is necessary in the submission.

7. Comparison to predicate device and conclusion

The technological characteristics, features, specifications, materials, and intended use of IPL Hair Remover, Model: G993, G996, G998 and G885 is the same or similar to the predicate devices quoted above.

The differences between the subject device and predicate devices do not raise new issues of safety or effectiveness.

| Elements of

Comparison	Subject Device	Predicate Device I	Predicate Device II	Predicate Device III	Remark
Device Name and
Model	IPL Hair Remover,
Model: G993, G996,
G998 and G885	Ipulse Smoothskin
Gold Hair Removal
Device	Lumilisse IPL Hair
Remover	Aimanfun Lumea
Comfort (Model: A-

                                                                                                                                                                                                                                                                                                                                                              |                   |

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Sponsor: Shenzhen Mywin Technology Co., Ltd. Subject Device: IPL Hair Remover, Model: G993, G996, G998 and G885 510(k) number: K211368

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Sponsor: Shenzhen Mywin Technology Co., Ltd. IPL Hair Remover, Model: G993, G996, G998 and G885 Subject Device: 510(k) number: K211368

Comparison in Detail(s):

Note 1:

Although there is difference about Type of use between Subject device and Predicate device I to III and provide additional description for using direction requirement under the direction of a

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Shenzhen Mywin Technology Co., Ltd. Sponsor: Subject Device: IPL Hair Remover, Model: G993, G996, G998 and G885 510(k) number: K211368

physician, after training by a healthcare professional. But the type of use of IPL Hair Remover is same to predicate device III (K190820). This difference does not affect the safety and effectiveness.

Note 2:

"Power Source(s)", "Weight", "Dimensions" is belong to basic characteristics. Although it is a little different from the predicate devices, it will not affect the main function and the intended use of the device. They all also comply with IEC 60601-1 requirements. So the differences will not raise any safety or effectiveness issue.

Note 3:

Although there is difference about Type of use between Subject device and supplement device,

the subject device provide additional description for using direction requirement that a selective photothermal treatment under the direction of a physician, after training by a healthcare professional. And the type of use of subject device is same to predicate device III (Prescription for use) referring to K190820. This difference does not affect the safety and effectiveness.

Note 4:

Although the wavelength of subject device is a little different from the predicate devices, but they all comply with IEC 60601-1, IEC 60601-2-57 requirement.

And the wavelength of subject device is same with that of predicted device I, and in the range of both predicted device I and predicted device III. So we believe that the wavelength (510-1100 nm) is effective in hair removal application and its safety is acceptable.

So the differences of wavelength will not raise any safety or effectiveness issue.

Note 5:

The types of "Spot Size (cm2)" of subject device, and there is minor difference between the subject device and the predicate devices. The spot size only affect the treatment skin area at one shot of flash. It do not affect the safety and effectiveness of the device. And they all comply with IEC 60601-1, IEC60601-2-57 requirement.

So the differences of Spot size will not raise any safety or effectiveness issue.

Note 6:

For "Light Intensity in each level" of subject device, and there is minor difference between the subject device and the predicate device I. But the light intensity of subject device is same to the predicate device II and predicate device III. So we believe that the light intensity (1.8-4.5 J/cm²)

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is effective in hair removal application and its safety is acceptable. And they all comply with IEC 60601-1, IEC60601-2-57 requirement.

So the differences of light intensity will not raise any safety or effectiveness issue.

Note 7

Although the pulse duration is minor different to predicate device I; but in the predicate device III (K 190820), its pulse duration is 3 milliseconds, which is identical to the pulse duration of 3 ms in subject device. And the photothermolysis treatment mainly is depended on its pulse output energy, and subject device's output energy is substantial equivalent to others predicate device. So the minor difference on pulse duration do not affect the safety and effectiveness.

Finial Conclusion:

Based on the nonclinical testing conducted, the subject device "IPL Hair Remover, Model: G993, G996, G998 and G885" is the same or similar to all predicate devices, as safe, as effective, and performs as well as the legally marketed predicate devices.