Fidia Pharmaceutical Corp.
United StatesFDA applicant, unverified
- Devices
- 10
What Fidia Pharmaceutical Corp. makes
Fidia Pharmaceutical Corp. manufactures a range of hydrogel-based wound care products, including BIONECT hydrogel foam, gauze pads, spray, clear hydrogel, and a BIONECT cream, as well as modified versions of these items.
These devices are classified as unclassified (Class U) and are listed in the FDA 510(k) database. The company is based in the United States.
Catalogue
Bionect Hydrogel Foam Ref K973722
Regimes: 510(k) Registry: 510(k)Modification Of Bionect Hydrogel Gauze Pads Ref K984262
Regimes: 510(k) Registry: 510(k)Modification Of Bionect Hydrogel Spray Ref K984266
Regimes: 510(k) Registry: 510(k)Modification Of Bionect Hydrogel Foam Ref K984267
Regimes: 510(k) Registry: 510(k)Bionect Hydrogel Ref K984413
Regimes: 510(k) Registry: 510(k)Bionect Hydrogel Gauze Pads Ref K973721
Regimes: 510(k) Registry: 510(k)Bionect Cream Ref K963004
Regimes: 510(k) Registry: 510(k)Bionect Hydrogel Spray Ref K973724
Regimes: 510(k) Registry: 510(k)Bionect Clear Hydrogel Ref K973725
Regimes: 510(k) Registry: 510(k)Modification Of Bionect Clear Hydrogel Ref K984264
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Fidia Pharmaceutical Corp. have in the registry?
The registry currently lists 10 devices for Fidia Pharmaceutical Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Fidia Pharmaceutical Corp.'s devices?
Among its 10 most recently registered devices, Fidia Pharmaceutical Corp. has devices listed in FDA 510(k) (10 devices).
What are the newest devices from Fidia Pharmaceutical Corp. in the registry?
The most recently registered devices listed for Fidia Pharmaceutical Corp. include BIONECT HYDROGEL FOAM, MODIFICATION OF BIONECT HYDROGEL GAUZE PADS, MODIFICATION OF BIONECT HYDROGEL SPRAY and MODIFICATION OF BIONECT HYDROGEL FOAM.