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 15, 2026, FDA's public records list Shenzhen GSD Tech Co., Ltd. with 7 510(k) clearances. The most recent is a 510(k) clearance dated Mar 3, 2023: Light Based Hair Removal Device GP592.
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.
| Mar 3, 2023 | Light Based Hair Removal Device GP592K230060 · OHT | 510(k) clearances |
| Dec 22, 2021 | Diode Laser System GP900A8, Diode Laser System GP900Q8K213225 · GEX | 510(k) clearances |
| Dec 15, 2020 | 308nm Excimer UV-light Skin Therapy SystemK202827 · FTC | 510(k) clearances |
| Sep 12, 2019 | CO2 Laser SystemK191518 · GEX | 510(k) clearances |
| May 11, 2018 | Light based hair removal deviceK180383 · OHT | 510(k) clearances |
| Apr 17, 2015 | DIODE LASER HAIR REMOVAL SYSTEMK142186 · GEX | 510(k) clearances |
| Nov 16, 2009 | GSD INTENSE PULSED LIGHT SYSTEM, MODELS: GP666C4, GP666CK091664 · ONF | 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
