Pcca, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Pcca, Inc. makes
Pcca, Inc. manufactures MucoLock Oral Gel, a medical device designed for oral mucosal protection and adhesion, intended to support wound healing or barrier formation in the mouth.
The company’s portfolio is regulated under the FDA’s Class II (U) designation, with devices authorised via the 510(k) pathway. MucoLock Oral Gel is listed in the FDA’s 510(k) registry. The manufacturer is based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
MucoLock Oral Gel Ref K203091
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Pcca, Inc. have in the registry?
The registry currently lists 2 devices for Pcca, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Pcca, Inc.'s devices?
Among its 2 most recently registered devices, Pcca, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Pcca, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Pcca, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Pcca, Inc. in the registry?
The most recently registered devices listed for Pcca, Inc. include Plum Vagiceuticals™ Vaginal Moisturizing Suppositories and MucoLock Oral Gel.