Protector, Inc.
United StatesFDA applicant, unverified
- Devices
- 3
What Protector, Inc. makes
Protector, Inc. manufactures dental instruments, including forceps for dressings, mouth mirrors, and operative explorers, designed for oral healthcare procedures.
These devices are classified as Class I under FDA regulations and are listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Forceps, Dressing, Dental Ref K925889
Regimes: 510(k) Registry: 510(k)Mirror, Mouth Ref K925890
Regimes: 510(k) Registry: 510(k)Explorer, Operative Ref K925888
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Protector, Inc. have in the registry?
The registry currently lists 3 devices for Protector, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Protector, Inc.'s devices?
Among its 3 most recently registered devices, Protector, Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do Protector, Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Protector, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Protector, Inc. in the registry?
The most recently registered devices listed for Protector, Inc. include FORCEPS, DRESSING, DENTAL, MIRROR, MOUTH and EXPLORER, OPERATIVE.