Medafor, Inc.
United StatesFDA applicant, unverified
- Devices
- 4
What Medafor, Inc. makes
Medafor, Inc. manufactures hemostatic products including Hemaderm containing Hemadex clotting beads, Hemaderm, Instaclot for over-the-counter use, and Traumastat for prescription use. The company also produces the Medafor Direct Gas-Assisted Application System for delivering these hemostatic agents.
These devices are classified as Class I and Class II medical devices and are listed in the FDA 510(k) registry. Medafor, Inc. is based in the United States.
Catalogue
Hemaderm Cotaining Hemadex Clotting Beads Ref K021678
Regimes: 510(k) Registry: 510(k)Medafor Direct Gas-Assisted Application System Ref K123325
Regimes: 510(k) Registry: 510(k)Hemaderm Ref K033666
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Medafor, Inc. have in the registry?
The registry currently lists 4 devices for Medafor, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Medafor, Inc.'s devices?
Among its 4 most recently registered devices, Medafor, Inc. has devices listed in FDA 510(k) (4 devices).
What risk classes do Medafor, Inc.'s devices fall under?
Among its 4 most recently registered devices, the classes recorded for Medafor, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Medafor, Inc. in the registry?
The most recently registered devices listed for Medafor, Inc. include HEMADERM COTAINING HEMADEX CLOTTING BEADS, Medafor Direct Gas-Assisted Application System, HEMADERM and INSTACLOT FOR OTC USE, TRAUMASSTAT FOR PRESCRIPTION USE.