Dermatec, Inc.
United StatesFDA applicant, unverified
- Devices
- 4
What Dermatec, Inc. makes
Dermatec, Inc. manufactures single-use wound care products, including burn pads for thermal injuries, transparent film dressings for monitoring wounds, zone transparent dressings for larger or multi-area coverage, and sterile finger bandages for minor cuts or abrasions.
These products are classified as Class I medical devices under FDA regulations and are supported by 510(k) clearance records in the U.S. registry. The company is based in the United States.
Catalogue
Dermatec Burn Pads Ref K863379
Regimes: 510(k) Registry: 510(k)Dermatec Transparent Film Dressing Ref K863580
Regimes: 510(k) Registry: 510(k)Dermatec Zone Transparent Dressing Ref K863578
Regimes: 510(k) Registry: 510(k)Dermatex Sterile Finger Bandage Ref K833638
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Dermatec, Inc. have in the registry?
The registry currently lists 4 devices for Dermatec, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Dermatec, Inc.'s devices?
Among its 4 most recently registered devices, Dermatec, Inc. has devices listed in FDA 510(k) (4 devices).
What risk classes do Dermatec, Inc.'s devices fall under?
Among its 4 most recently registered devices, the classes recorded for Dermatec, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Dermatec, Inc. in the registry?
The most recently registered devices listed for Dermatec, Inc. include DERMATEC BURN PADS, DERMATEC TRANSPARENT FILM DRESSING, DERMATEC ZONE TRANSPARENT DRESSING and DERMATEX STERILE FINGER BANDAGE.