(30 days)
Not Found
No.
The document makes no mention of AI, ML, or DNN, nor does it describe any function that inherently requires such technologies. The device operates as a direct laser energy source with user-set parameters via a touchscreen.
Yes
The device is used for surgical applications like vaporization, incision, excision, ablation, cutting, hemostasis, coagulation of soft tissue, and laser-assisted lipolysis, which are all therapeutic interventions.
No
The device is indicated for surgical applications (vaporization, incision, excision, ablation, cutting, hemostasis, coagulation) and laser-assisted lipolysis, which are therapeutic rather than diagnostic actions.
No
The device is a medical diode laser system that produces therapeutic effects through laser energy and includes physical components like the main unit, foot switch, power cord, protective goggles, and an LCD touchscreen. It explicitly describes hardware components and their functions, clearly indicating it is not a software-only device.
No
The device is a surgical laser intended for direct tissue modification (vaporization, incision, excision, etc.), not for examining specimens derived from the human body to provide information for diagnosis or treatment.
N/A
Intended Use / Indications for Use
The Medical Diode Laser (Model: MZ-GK) is indicated for use in surgical applications requiring the vaporization, incision, excision, ablation, cutting and hemostasis, or coagulation of soft tissue in conjunction with endoscopic equipment for medical specialist including: Urology, Thoracic Surgery, Plastic Surgery and Dermatology, General Surgery, Ophthalmology, Orthopedics, Podiatry, Arthroscopy, Spinal Surgery, Gynecology, Pulmonary Surgery, Neurosurgery, Gastroenterology, Head/neck/ENT and Radiology, Oral Surgery and Dental procedures, Endovascular coagulation and endovenous occlusion of the greater saphenous vein in patients with superficial vein reflux. The Medical Diode Laser (Model: MZ-GK) is further indicated for laser assisted lipolysis.
The Medical Diode Laser (Model: MZ-K20) is indicated for:
- Incision, excision, ablation, vaporization, hemostasis and/or coagulation of soft tissue.
- Endovascular coagulation and endovenous occlusion of the greater saphenous vein in patients with superficial vein reflux.
The Medical Diode Laser (Model: MZ-N75) is intended to incision, excision, ablation, vaporization, hemostasis and/or coagulation of soft tissue.
Product codes
GEX
Device Description
The Medical Diode Laser (Models: MZ-GK, MZ-K20, MZ-N75) incorporates a solid state diode as laser energy source for producing its therapeutic effects, it is designed to deliver continuous or pulsed, infrared laser energy at wavelengths of 980nm and 1470nm respectively for MZ-GK, 1470nm for MZ-K20 and 1940nm for MZ-N75. The device also incorporates a red (650nm) or green(532nm) aiming beam diode to indicate the area to be irradiated by the laser beam. The device is composed of the main unit, foot switch, power cord, and protective goggles. The device incorporates an LCD touchscreen for the device user to set output parameters and for control of the device. The device transmits the laser output via third-party optical fibers with SMA905 connectors and with single cores of 200μm, 300μm, 400μm, 600μm, 800μm and 1000μm diameter respectively.
Mentions image processing
Not Found
Mentions AI, DNN, or ML
Not Found
Input Imaging Modality
Not Found
Anatomical Site
Soft tissue
Indicated Patient Age Range
Not Found
Intended User / Care Setting
Medical specialist including: Urology, Thoracic Surgery, Plastic Surgery and Dermatology, General Surgery, Ophthalmology, Orthopedics, Podiatry, Arthroscopy, Spinal Surgery, Gynecology, Pulmonary Surgery, Neurosurgery, Gastroenterology, Head/neck/ENT and Radiology, Oral Surgery and Dental procedures.
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)
Non-clinical data:
Electrical Compatibility and Electrical Safety: The Medical Diode Laser was tested and found to conform to the criteria of IEC 60601-1:2005+AMD1:2012+AMD2:2020 and IEC 60601-1-2:2014+A1:2020.
Performance Testing – Bench: Pioon has conducted functional and system level testing to validate the performance of the devices. The results of the bench testing show that the subject device meets its accuracy specifications and meets relevant consensus standards, including IEC 60825-1:2014 and IEC 60601-2-22:2019.
Software Verification and Validation Testing: Software verification and validation testing were conducted and documentation was provided as recommended by FDA's Guidance for Industry and FDA Staff, "Content of Premarket Submissions for Device Software Function". The Documentation Level was considered as a "Basic Documentation Level".
Key Metrics (Sensitivity, Specificity, PPV, NPV, etc.)
Not Found
Predicate Device(s)
Reference Device(s)
Not Found
Predetermined Change Control Plan (PCCP) - All Relevant Information
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.
FDA 510(k) Clearance Letter - Medical Diode Laser
Page 1
U.S. Food & Drug Administration
10903 New Hampshire Avenue Doc ID# 04017.07.05
Silver Spring, MD 20993
www.fda.gov
April 4, 2025
Wuhan Pioon Technology Co.,Ltd.
Tracy Liu
Regulatory Affairs
12th Floor, Building 1, Innovative Unit, R&D Center Project,
Marine World Shipyard Park, No. 16 Fozuling 3rd Road, East L
Wuhan, Hubei 430205
China
Re: K250656
Trade/Device Name: Medical Diode Laser (Models: MZ-GK, MZ-K20, MZ-N75)
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: GEX
Dated: March 3, 2025
Received: March 5, 2025
Dear Tracy Liu:
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 (the 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 available 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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K250656 - Tracy Liu Page 2
Additional information about changes that may require a new premarket notification are provided in the FDA guidance documents entitled "Deciding When to Submit a 510(k) for a Change to an Existing Device" (https://www.fda.gov/media/99812/download) and "Deciding When to Submit a 510(k) for a Software Change to an Existing Device" (https://www.fda.gov/media/99785/download).
Your device is also subject to, among other requirements, the Quality System (QS) regulation (21 CFR Part 820), which includes, but is not limited to, 21 CFR 820.30, Design controls; 21 CFR 820.90, Nonconforming product; and 21 CFR 820.100, Corrective and preventive action. Please note that regardless of whether a change requires premarket review, the QS regulation requires device manufacturers to review and approve changes to device design and production (21 CFR 820.30 and 21 CFR 820.70) and document changes and approvals in the device master record (21 CFR 820.181).
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); medical device reporting (reporting of medical device-related adverse events) (21 CFR Part 803) for devices or postmarketing safety reporting (21 CFR Part 4, Subpart B) for combination products (see https://www.fda.gov/combination-products/guidance-regulatory-information/postmarketing-safety-reporting-combination-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 Part 4, Subpart A) for combination products; and, if applicable, the electronic product radiation control provisions (Sections 531-542 of the Act); 21 CFR Parts 1000-1050.
All medical devices, including Class I and unclassified devices and combination product device constituent parts are required to be in compliance with the final Unique Device Identification System rule ("UDI Rule"). The UDI Rule requires, among other things, that a device bear a unique device identifier (UDI) on its label and package (21 CFR 801.20(a)) unless an exception or alternative applies (21 CFR 801.20(b)) and that the dates on the device label be formatted in accordance with 21 CFR 801.18. The UDI Rule (21 CFR 830.300(a) and 830.320(b)) also requires that certain information be submitted to the Global Unique Device Identification Database (GUDID) (21 CFR Part 830 Subpart E). For additional information on these requirements, please see the UDI System webpage at https://www.fda.gov/medical-devices/device-advice-comprehensive-regulatory-assistance/unique-device-identification-system-udi-system.
Also, please note the regulation entitled, "Misbranding by reference to premarket notification" (21 CFR 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-devices/medical-device-safety/medical-device-reporting-mdr-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/medical-devices/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.
Page 3
K250656 - Tracy Liu Page 3
See the DICE website (https://www.fda.gov/medical-devices/device-advice-comprehensive-regulatory-assistance/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,
TANISHA L. HITHE -S
Digitally signed by TANISHA L. HITHE -S
Date: 2025.04.04 18:11:24 -04'00'
Tanisha Hithe
Assistant Director
DHT4A: Division of General Surgery Devices
OHT4: Office of Surgical and Infection Control Devices
Office of Product Evaluation and Quality
Center for Devices and Radiological Health
Enclosure
Page 4
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Food and Drug Administration
Indications for Use
Form Approved: OMB No. 0910-0120
Expiration Date: 07/31/2026
See PRA Statement below.
510(k) Number (if known): K250656
Device Name: Medical Diode Laser (Models: MZ-GK, MZ-K20, MZ-N75)
Indications for Use (Describe)
The Medical Diode Laser (Model: MZ-GK) is indicated for use in surgical applications requiring the vaporization, incision, excision, ablation, cutting and hemostasis, or coagulation of soft tissue in conjunction with endoscopic equipment for medical specialist including: Urology, Thoracic Surgery, Plastic Surgery and Dermatology, General Surgery, Ophthalmology, Orthopedics, Podiatry, Arthroscopy, Spinal Surgery, Gynecology, Pulmonary Surgery, Neurosurgery, Gastroenterology, Head/neck/ENT and Radiology, Oral Surgery and Dental procedures, Endovascular coagulation and endovenous occlusion of the greater saphenous vein in patients with superficial vein reflux. The Medical Diode Laser (Model: MZ-GK) is further indicated for laser assisted lipolysis.
The Medical Diode Laser (Model: MZ-K20) is indicated for:
- Incision, excision, ablation, vaporization, hemostasis and/or coagulation of soft tissue.
- Endovascular coagulation and endovenous occlusion of the greater saphenous vein in patients with superficial vein reflux.
The Medical Diode Laser (Model: MZ-N75) is intended to incision, excision, ablation, vaporization, hemostasis and/or coagulation of soft tissue.
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)
CONTINUE ON A SEPARATE PAGE IF NEEDED.
This section applies only to requirements of the Paperwork Reduction Act of 1995.
DO NOT SEND YOUR COMPLETED FORM TO THE PRA STAFF EMAIL ADDRESS BELOW.
The burden time for this collection of information is estimated to average 79 hours per response, including the time to review instructions, search existing data sources, gather and maintain the data needed and complete and review the collection of information. Send comments regarding this burden estimate or any other aspect of this information collection, including suggestions for reducing this burden, to:
Department of Health and Human Services
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"An agency may not conduct or sponsor, and a person is not required to respond to, a collection of information unless it displays a currently valid OMB number."
Page 5
510(k) Summary
In accordance with the content and format regulatory requirements of 21 CFR Part 807.92, the 510(k) Summary for the Medical Diode Laser is provided below. The assigned 510(k) Number: K250656
1. Submitter
Device Submitter: Wuhan Pioon Technology Co., Ltd.
Address: 12th Floor, Building 1, Innovative Unit, R&D Center Project, Marine World Shipyard Park, No. 16 Fozuling 3rd Road, East Lake High-tech Development Zone, 430205, Wuhan, Hubei, China
Tel: +86 27 81783687
Contact Person: Zhang Feng, Management Representative
Phone: +86 18062448535
E-mail: zhangfeng@pioon.com
Date Prepared: April 3, 2025
Official Correspondent: Tracy Liu, Wuhan Pioon Technology Co., Ltd.
Phone: +86 15012997429
Email: tracy@pioon.com
2. Device
Type of 510(k) submission: Special
Device name: Medical Diode Laser (Models: MZ-GK, MZ-K20, MZ-N75)
Common Name: Powered Laser Surgical Instrument
Regulation: 878.4810 - Laser surgical instrument for use in general and plastic surgery and in dermatology
Medical Specialty: General & Plastic Surgery
Regulatory Class: II
Product Code: GEX
3. Predicate Device
| Item | Predicate Device 1 | Predicate Device 2 | Predicate Device 3 |
|---|---|---|---|
| 510(k) Number | K240747 | K240179 | K230274 |
Page 6
The predicates have not been subject to a design-related recall. No reference devices were used in this submission.
4. Device Description
The Medical Diode Laser (Models: MZ-GK, MZ-K20, MZ-N75) incorporates a solid state diode as laser energy source for producing its therapeutic effects, it is designed to deliver continuous or pulsed, infrared laser energy at wavelengths of 980nm and 1470nm respectively for MZ-GK, 1470nm for MZ-K20 and 1940nm for MZ-N75. The device also incorporates a red (650nm) or green(532nm) aiming beam diode to indicate the area to be irradiated by the laser beam. The device is composed of the main unit, foot switch, power cord, and protective goggles. The device incorporates an LCD touchscreen for the device user to set output parameters and for control of the device. The device transmits the laser output via third-party optical fibers with SMA905 connectors and with single cores of 200μm, 300μm, 400μm, 600μm, 800μm and 1000μm diameter respectively.
5. Indications for Use
The Medical Diode Laser (Model: MZ-GK) is indicated for use in surgical applications requiring the vaporization, incision, excision, ablation, cutting and hemostasis, or coagulation of soft tissue in conjunction with endoscopic equipment for medical specialist including: Urology, Thoracic Surgery, Plastic Surgery and Dermatology, General Surgery, Ophthalmology, Orthopedics, Podiatry, Arthroscopy, Spinal Surgery, Gynecology, Pulmonary Surgery, Neurosurgery, Gastroenterology, Head/neck/ENT and Radiology, Oral Surgery and Dental procedures, Endovascular coagulation and endovenous occlusion of the greater saphenous vein in patients with superficial vein reflux. The Medical Diode Laser (Model: MZ-GK) is further indicated for laser assisted lipolysis.
The Medical Diode Laser (Model: MZ-K20) is indicated for:
- Incision, excision, ablation, vaporization, hemostasis and/or coagulation of soft tissue.
- Endovascular coagulation and endovenous occlusion of the greater saphenous vein in patients with superficial vein reflux.
The Medical Diode Laser (Model: MZ-N75) is intended to incision, excision, ablation, vaporization, hemostasis and/or coagulation of soft tissue.
6. Comparison to the Predicate Device
The Medical Diode Laser (Models: MZ-GK, MZ-K20, MZ-N75), has been compared to the Medical Diode Laser (Model: M2-GK) (K240747), Medical Diode Laser (Model: L2) (K240179)
| Device Name | Medical Diode Laser (M2-GK) | Medical Diode Laser (Model:L2) | Medical Diode Laser (M2) |
|---|---|---|---|
| Submitter | Wuhan Pioon Technology Co., Ltd. | Wuhan Pioon Technology Co., Ltd. | Wuhan Pioon Technology Co., Ltd. |
| Product Code | GEX | GEX | GEX |
Page 7
and Medical Diode Laser (Model: M2)(K230274) respectively as reference for substantial equivalence. A table comparing the predicate devices to the subject device is shown as the following:
| Item | Subject Device (this submission) | Predicate Device 1 (K240747) | Predicate Device 2 (K240179) | Predicate Device 3 (K230274) |
|---|---|---|---|---|
| Trade Name | Medical Diode Laser | Medical Diode Laser | Medical Diode Laser | Medical Diode Laser |
| Model | MZ-GK, MZ-K20, MZ-N75 | M2-GK | L2 | M2 |
| Product Code | GEX | GEX | GEX | GEX |
| Regulation NO. | 21 CFR 878.4810 | 21 CFR 878.4810 | 21 CFR 878.4810 | 21 CFR 878.4810 |
| Class | II | II | II | II |
| Indications for Use | The Medical Diode Laser (Model: MZ-GK) is indicated for use in surgical applications requiring the vaporization, incision, excision, ablation, cutting and hemostasis, or coagulation of soft tissue in conjunction with endoscopic equipment for medical specialist including: Urology, Thoracic Surgery, Plastic Surgery and Dermatology, General Surgery, Ophthalmology, Orthopedics, Podiatry, Arthroscopy, Spinal Surgery, Gynecology, Pulmonary Surgery, Neurosurgery, Gastroenterology, Head/neck/ENT and Radiology, Oral Surgery and Dental procedures, | The Medical Diode Laser(Model: M2-GK) is indicated for use in surgical applications requiring the vaporization, incision, excision, ablation, cutting and hemostasis, or coagulation of soft tissue in conjunction with endoscopic equipment for medical specialist including: Urology, Thoracic Surgery, Plastic Surgery and Dermatology, General Surgery, Ophthalmology, Orthopedics, Podiatry, Arthroscopy, Spinal Surgery, Gynecology, Pulmonary Surgery, Neurosurgery, Gastroenterology, Head/neck/ENT and | The Medical Diode Laser (Model: L2) is indicated for: -Incision, excision, ablation, vaporization, hemostasis and/or coagulation of soft tissue. -Endovascular coagulation and endovenous occlusion of the greatest saphenous vein in patients with superficial vein reflux. | Medical Diode Laser is intended to incision, excision, ablation, vaporization, hemostasis and/or coagulation of soft tissue. |
Page 8
| Item | Subject Device (this submission) | Predicate Device 1 (K240747) | Predicate Device 2 (K240179) | Predicate Device 3 (K230274) |
|---|---|---|---|---|
| Indications for Use (continued) | Endovascular coagulation and endovenous occlusion of the greater saphenous vein in patients with superficial vein reflux. The Medical Diode Laser (Model: MZ-GK) is further indicated for laser assisted lipolysis. The Medical Diode Laser (Model: MZ-K20) is indicated for: -Incision, excision, ablation, vaporization, hemostasis and/or coagulation of soft tissue. -Endovascular coagulation and endovenous occlusion of the greater saphenous vein in patients with superficial vein reflux. The Medical Diode Laser (Model: MZ-N75) is intended to incision, excision, ablation, vaporization, hemostasis and/or coagulation of soft tissue. | Radiology, Oral Surgery and Dental procedures, Endovascular coagulation and endovenous occlusion of the greater saphenous vein in patients with superficial vein reflux. The Medical Diode Laser (Model: M2-GK) is further indicated for laser assisted lipolysis. | ||
| Use of Device | Rx only | Rx only | Rx only | Rx only |
| Laser Type | Diode laser | Diode laser | Diode laser | Diode laser |
| Laser Classification | Class IV | Class IV | Class IV | Class IV |
| Configuration | Main Unit | Main Unit | Main Unit | Main Unit |
Page 9
| Item | Subject Device (this submission) | Predicate Device 1 (K240747) | Predicate Device 2 (K240179) | Predicate Device 3 (K230274) |
|---|---|---|---|---|
| Foot Control | Foot Control | Foot Control | Foot Control | |
| Laser Wavelength | MZ-GK: 980nm, 1470nm MZ-K20: 1470nm MZ-N75: 1940nm | 980nm 1470nm | 1470nm | 1940nm |
| Max Power | MZ-GK: 30W-980nm, 15W-1470nm MZ-K20: Up to 20W MZ-N75: Up to 7.5W | 30W-980nm 15W-1470nm | Up to 20W | Up to 7.5W |
| Operation Mode | CW and Pulse | CW and Pulse | CW and Pulse | CW and Pulse |
| Pulse Duration | MZ-GK: 10 ms – 1s MZ-K20: CW or 10 ms – 10 s MZ-N75: CW or 10 ms – 10 s | 10 ms – 1s | CW or 10 ms – 10 s | CW or 10 ms – 10 s |
| Repetition Rate | MZ-GK: 0.5 to 50 Hz MZ-K20: CW or up to 100 Hz MZ-N75: CW or up to 100 Hz | 0.5 to 50 Hz | CW or up to 100 Hz | CW or up to 100 Hz |
| Aiming Beam | Green 532nm ( |