Proact, Inc.
United StatesFDA applicant, unverified
- Devices
- 7
What Proact, Inc. makes
Proact, Inc. manufactures the Proact with Gel and Proact 1, which are medical devices designed for wound care, likely intended for the application of topical treatments to promote healing in chronic or acute wounds.
These devices are classified as Class II under FDA regulations and are listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Proact 1 Ref K003909
Regimes: 510(k) Registry: 510(k)Quick Core Ii Ref K941256
Regimes: 510(k) Registry: 510(k)Proact Biopsy Needle Enchancements Ref K926559
Regimes: 510(k) Registry: 510(k)Bauer Temno Biopsy Needle Ref K902319
Regimes: 510(k) Registry: 510(k)Bone-Temno/Sternum-Temno Ref K913306
Regimes: 510(k) Registry: 510(k)Bauer Flexi-Temno Biopsy Needle Ref K902320
Regimes: 510(k) Registry: 510(k)Proact With Gel Or Proact 1 Ref K052243
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Proact, Inc. have in the registry?
The registry currently lists 7 devices for Proact, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Proact, Inc.'s devices?
Among its 7 most recently registered devices, Proact, Inc. has devices listed in FDA 510(k) (7 devices).
What risk classes do Proact, Inc.'s devices fall under?
Among its 7 most recently registered devices, the classes recorded for Proact, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Proact, Inc. in the registry?
The most recently registered devices listed for Proact, Inc. include PROACT 1, QUICK CORE II, PROACT BIOPSY NEEDLE ENCHANCEMENTS and BAUER TEMNO BIOPSY NEEDLE.