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Medtek Skin Care, Inc.

Also registered as Medtek Skincare, LLC

United Statesfrom the FDA registration address FDA establishment FEI 1318319

Devices
2
Registrations
FDA
FDA recalls
0

Catalogue2

Newest first, rows 1-2 of 2

  • Poly Rejuv Ref K180875

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Poly Clear Ref K183708

    Active Regimes: 510(k) Registry: 510(k) Class:II

Company details

FDA FEI number
1318319
Address
3 Depot St, HUDSON FALLS, NY, 12839

Frequently asked questions

How many devices does Medtek Skin Care, Inc. have in the registry?

The registry currently lists 2 devices for Medtek Skin Care, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Medtek Skin Care, Inc.'s devices?

Among its 2 most recently registered devices, Medtek Skin Care, Inc. has devices listed in FDA 510(k) (2 devices).

What risk classes do Medtek Skin Care, Inc.'s devices fall under?

Among its 2 most recently registered devices, the classes recorded for Medtek Skin Care, Inc.'s devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from Medtek Skin Care, Inc. in the registry?

The most recently registered devices listed for Medtek Skin Care, Inc. include POLY REJUV and Poly Clear.

Generated automatically from registry data and not verified by a human reviewer.

This is an FDA establishment record. No EUDAMED registration is known for this company and no recalls are recorded.