Dermarx Corp.
United StatesFDA applicant, unverified
- Devices
- 4
What Dermarx Corp. makes
Dermarx Corp. makes wound care products including gels, hydrogel gauze dressings, foam island dressings, and absorbent dressings such as DERMAMEND GEL, DERMAMEND HYDROGEL GAUZE DRESSING, DERMAMEND FOAM ISLAND DRESSING, and DYNASORB.
These devices are classified as Class I and unclassified (U) medical devices and are listed in the FDA 510(k) registry. The company is based in the United States.
Catalogue
Dermamend Gel Ref K962089
Regimes: 510(k) Registry: 510(k)Dermamend Hydrogel Gauze Dressing Ref K972336
Regimes: 510(k) Registry: 510(k)Dynasorb Ref K951561
Regimes: 510(k) Registry: 510(k)Dermamend Foam Island Dressing Ref K970600
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Dermarx Corp. have in the registry?
The registry currently lists 4 devices for Dermarx Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Dermarx Corp.'s devices?
Among its 4 most recently registered devices, Dermarx Corp. has devices listed in FDA 510(k) (4 devices).
What risk classes do Dermarx Corp.'s devices fall under?
Among its 4 most recently registered devices, the classes recorded for Dermarx Corp.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Dermarx Corp. in the registry?
The most recently registered devices listed for Dermarx Corp. include DERMAMEND GEL, DERMAMEND HYDROGEL GAUZE DRESSING, DYNASORB and DERMAMEND FOAM ISLAND DRESSING.