Depilase Group , Ltd.: FDA filings under this applicant name

FDA lists 7 510(k) clearances under the applicant name “Depilase Group , Ltd.” (first 2000, latest 2003), across 1 product code in 1 review panel. Median 510(k) review time under this name: 79 days. Related companies, subsidiaries and acquired businesses that file under other applicant names are counted on their own pages, not here.

510(k) clearances per year

YearClearancesMedian review days
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Top product codes

Product codeDeviceSubmissions510(k) clearances
GEXPowered Laser Surgical Instrument77

Review panels

Most recent Depilase Group , Ltd. 510(k) clearances

510(k)DeviceProduct codeDecision dateReview days
K030508DEPILASE TRIO LASE LASER SYSTEMGEX2003-05-2090
K030510DEPILASE TWIN YAG LASER SYSTEMGEX2003-05-1484
K030506DEPILASE YAG LASE PLUS LASER SYSTEMGEX2003-05-0979
K020697DEPILASE TWIN YAG LASER SYSTEMGEX2002-04-1239
K020463DEPILASE YAG LASE PLUS LASER SYSTEMGEX2002-02-2715
K020412DEPILASE TWIN LASE LASER SYSTEMGEX2002-02-2215
K001990DEPILASE YAGLASE ND:YAG LASER SYSTEM AND ACCESSORIESGEX2000-10-23116

Recalls

openFDA lists no recalls under a recalling firm named Depilase Group , Ltd..

Recalling firms are matched to this applicant name by name only (same normalization), so related entities that recall under another name are not counted. A recall count says nothing about how safe one company's devices are compared with another's.

Frequently asked questions

How many FDA 510(k) clearances are listed under Depilase Group , Ltd.?

FDA lists 7 510(k) clearances under the applicant name “Depilase Group , Ltd.” (first 2000, latest 2003), across 1 product code in 1 review panel. Filings under other applicant names, such as subsidiaries, are not included.

How long has FDA taken to clear 510(k)s filed by Depilase Group , Ltd.?

The median time from FDA receipt to decision across 510(k)s cleared under the name Depilase Group , Ltd. is 79 days.

Which FDA product codes appear under Depilase Group , Ltd.?

The most frequent FDA product codes under this applicant name are GEX (Powered Laser Surgical Instrument, 7).

Next steps

Data from openFDA (510(k), PMA, De Novo, device recalls), ClinicalTrials.gov and SEC company tickers. Each page covers one FDA applicant name (spelling variants such as punctuation and legal suffixes combined); filings under other names are not included. Review days run from FDA receipt to decision. Not regulatory advice. Report an error in this data.

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