Data / Medical devices / China / Beijing Adss Development Co., Ltd.
Beijing Adss Development Co., Ltd.: FDA-registered device maker in Beijing, China, 8 510(k) clearances
Beijing Adss Development Co., Ltd. is registered with the FDA (registration 3007084556) in Beijing, China. It lists 8 device types. The FDA files 8 510(k) clearances under its listings, the newest dated December 20, 2024. Registered through 2027. FDA data exported November 2, 2026.
SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.
- FDA registration number
- 3007084556
- Address
- Room 609, F6, Building 13, Yard 5 Tianhua Street Daxing District, Beijing, China, 102600
- Owner or operator
- Beijing ADSS Development Co., Ltd. (10053130)
- Roles
- Manufacturer
- First device listed
- December 27, 2016
- Registered through
- 2027
- Brand names listed
- Aphrona LED facial mask, Aqua Facial, Diode Laser Therapy Machine, Diode Laser Therapy System, Electromagnetic Stimulator Device, Fractional CO2 Laser Therapy System (FG900-S,FG900-S2,PhantomClear), Intensity Pulsed Light Therapy System, ND YAG Q-Switch Laser Therapy Machine FG2010 FG2010-B FG2014 and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Brush, Dermabrasion, Powered | GFE | 1 | Manufacturer | accessdata.fda.gov |
| Device, Skin Potential Measurement | HCJ | 2 | Manufacturer | accessdata.fda.gov |
| Light Based Over The Counter Wrinkle Reduction | OHS | 2 | Manufacturer | accessdata.fda.gov |
| Massager, Therapeutic, Electric | ISA | 1 | Manufacturer | accessdata.fda.gov |
| Over-The-Counter Powered Light Based Laser For Acne | OLP | 2 | Manufacturer | accessdata.fda.gov |
| Powered Laser Surgical Instrument | GEX | 2 | Manufacturer | accessdata.fda.gov |
| Powered Light Based Non-Laser Surgical Instrument With Thermal Effect | ONF | 2 | Manufacturer | accessdata.fda.gov |
| Stimulator, Muscle, Powered, For Muscle Conditioning | NGX | 2 | Manufacturer | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| December 20, 2024 | K241670 | Fractional CO2 Laser Therapy System (FG900-S); Fractional CO2 Laser Therapy System (FG900-S2) | GEX | Substantially Equivalent | Beijing Adss Development Co., Ltd. | accessdata.fda.gov |
| March 15, 2024 | K233307 | Intensity Pulsed Light Therapy System | ONF | Substantially Equivalent | Beijing Adss Development Co., Ltd. | accessdata.fda.gov |
| February 20, 2024 | K231896 | Diode Laser Therapy System | GEX | Substantially Equivalent | Beijing Adss Development Co., Ltd. | accessdata.fda.gov |
| July 7, 2023 | K231318 | Electromagnetic Stimulator Device(Model EM Contouring and Tesla Duet) | NGX | Substantially Equivalent | Beijing Adss Development Co., Ltd. | accessdata.fda.gov |
| August 23, 2022 | K220268 | Picosecond Laser System (Model PS10-A and PS10-B) | GEX | Substantially Equivalent | Beijing Adss Development Co., Ltd. | accessdata.fda.gov |
| May 1, 2020 | K192295 | PDT-FACE | OLP | Substantially Equivalent | Beijing Adss Development Co., Ltd. | accessdata.fda.gov |
| February 22, 2017 | K161926 | ND YAG Q-switch Laser Therapy Machine | GEX | Substantially Equivalent | Beijing Adss Development Co., Ltd. | accessdata.fda.gov |
| November 16, 2016 | K161692 | Diode Laser Therapy Machine | GEX | Substantially Equivalent | Beijing Adss Development Co., Ltd. | accessdata.fda.gov |
Compare with other makers
- All makers of Powered Laser Surgical Instrument
- All makers of Powered Light Based Non-Laser Surgical Instrument With Thermal Effect
- All makers of Device, Skin Potential Measurement
- All makers of Brush, Dermabrasion, Powered
- All makers of Massager, Therapeutic, Electric
- All makers of Stimulator, Muscle, Powered, For Muscle Conditioning
Updated December 20, 2024. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.