Combe, Inc.
United StatesFDA applicant, unverified
- Devices
- 6
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Cushions, Denture Adhesive, All-Day Ref K770413
Regimes: 510(k) Registry: 510(k)Fungus Fighter Insoles Ref K780719
Regimes: 510(k) Registry: 510(k)Sea-Bond Adhevise Denture Cushions Ref K770175
Regimes: 510(k) Registry: 510(k)Cfr Monograph Ref K925259
Regimes: 510(k) Registry: 510(k)Sea-Bond Ref K863375
Regimes: 510(k) Registry: 510(k)Otc Denture Cleanser Ref K942203
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Combe, Inc. have in the registry?
The registry currently lists 6 devices for Combe, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Combe, Inc.'s devices?
Among its 6 most recently registered devices, Combe, Inc. has devices listed in FDA 510(k) (6 devices).
What risk classes do Combe, Inc.'s devices fall under?
Among its 6 most recently registered devices, the classes recorded for Combe, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Combe, Inc. in the registry?
The most recently registered devices listed for Combe, Inc. include CUSHIONS, DENTURE ADHESIVE, ALL-DAY, FUNGUS FIGHTER INSOLES, SEA-BOND ADHEVISE DENTURE CUSHIONS and CFR MONOGRAPH.