Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in ChinaLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under its name, each linked to the record.
As of Nov 13, 2026, FDA's public records list Beijing ADSS Development with 10 510(k) clearances. The most recent is a 510(k) clearance dated Dec 20, 2024: Fractional CO2 Laser Therapy System (FG900-S); Fractional CO2 Laser Therapy System (FG90….
Drug approvals, 510(k) clearances, recalls and letters, 2017 to 2026 to date
A hatched bar is a year that is not over, so its count covers only part of the year.
| Date | Record | Source |
|---|---|---|
| Dec 20, 2024 | Fractional CO2 Laser Therapy System (FG900-S); Fractional CO2 Laser Therapy System (FG900-S2)K241670 · GEX | 510(k) clearances |
| Mar 15, 2024 | Intensity Pulsed Light Therapy SystemK233307 · ONF | 510(k) clearances |
| Feb 20, 2024 | Diode Laser Therapy SystemK231896 · GEX | 510(k) clearances |
| Jul 7, 2023 | Electromagnetic Stimulator Device(Model EM Contouring and Tesla Duet)K231318 · NGX | 510(k) clearances |
| Aug 23, 2022 | Picosecond Laser System (Model PS10-A and PS10-B)K220268 · GEX | 510(k) clearances |
| May 1, 2020 | PDT-FACEK192295 · OLP | 510(k) clearances |
| Feb 22, 2017 | ND YAG Q-switch Laser Therapy MachineK161926 · GEX | 510(k) clearances |
| Nov 16, 2016 | Diode Laser Therapy MachineK161692 · GEX | 510(k) clearances |
Spellings are joined only when they reduce to the same name, or a reviewed source names the same company. Sharing an FDA establishment number (FEI) is not enough: contract sites make products for many firms. Facts marked AI were labelled by a language model from the firm's FDA names; everything else comes from FDA or Wikidata. How this page is built
