Dentec, Inc.
United StatesFDA applicant, unverified
- Devices
- 3
What Dentec, Inc. makes
Dentec, Inc. manufactures dental devices including FIBERBOND, DENTEC 4000, and PERI MIRROR/SALIVA EJECTOR.
The company's products are regulated as Class I and Class II devices and are listed in the FDA 510(k) registry. Dentec, Inc. is based in the US.
Catalogue
Fiberbond Ref K864376
Regimes: 510(k) Registry: 510(k)Dentec 4000 Ref K894930
Regimes: 510(k) Registry: 510(k)Peri Mirror/Saliva Ejector Ref K833429
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Dentec, Inc. have in the registry?
The registry currently lists 3 devices for Dentec, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Dentec, Inc.'s devices?
Among its 3 most recently registered devices, Dentec, Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do Dentec, Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Dentec, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Dentec, Inc. in the registry?
The most recently registered devices listed for Dentec, Inc. include FIBERBOND, DENTEC 4000 and PERI MIRROR/SALIVA EJECTOR.