Cosmedtech, Inc.
United StatesFDA applicant, unverified
- Devices
- 3
What Cosmedtech, Inc. makes
Cosmedtech, Inc. manufactures medical devices for fluid aspiration, including cannulas and general-purpose aspirators designed for surgical and procedural applications. These products are intended for removing fluids, tissue, or debris during minimally invasive procedures.
The company’s portfolio is regulated under FDA Class II devices, with products listed via the 510(k) pathway. These devices are based in the United States.
Catalogue
Cannula And General Purpose Aspirator Ref K873552
Regimes: 510(k) Registry: 510(k)Cosmedtech General Aspirator Ref K870574
Regimes: 510(k) Registry: 510(k)Cosmedtech Cannula Ref K870560
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Cosmedtech, Inc. have in the registry?
The registry currently lists 3 devices for Cosmedtech, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Cosmedtech, Inc.'s devices?
Among its 3 most recently registered devices, Cosmedtech, Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do Cosmedtech, Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Cosmedtech, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Cosmedtech, Inc. in the registry?
The most recently registered devices listed for Cosmedtech, Inc. include CANNULA AND GENERAL PURPOSE ASPIRATOR, COSMEDTECH GENERAL ASPIRATOR and COSMEDTECH CANNULA.