Perimetrics, Inc
United Statesfrom the FDA registration address FDA establishment FEI 3039642990
- Devices
- 7
- Registrations
- FDA
- FDA recalls
- 0
What Perimetrics, Inc makes
Perimetrics, Inc. manufactures dental diagnostic tools, including a percussive analysis handpiece for assessing dental stability, its protective cover, and a complete system comprising a base station, handpiece, and smart tips for intraoral scanning.
The company’s devices are classified as Class I under FDA regulations and are listed in the FDA’s Unique Device Identifier (UDI) database. The manufacturer is based in the United States.
Catalogue
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
Perimetrics Periometer Ref K072213
Regimes: 510(k) Registry: 510(k)InnerView System Ref K251597
Regimes: 510(k) Registry: 510(k)InnerView LC Ref K232657
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3039642990
- Address
- 2961 W MacArthur Blvd, Suite 121, Santa Ana, CA, 92704
Frequently asked questions
How many devices does PERIMETRICS, INC have in the registry?
The registry currently lists 7 devices for PERIMETRICS, INC. Devices recorded under merged duplicate company entries are counted once.
Which registries list PERIMETRICS, INC's devices?
Among its 7 most recently registered devices, PERIMETRICS, INC has devices listed in FDA 510(k) (3 devices) and FDA GUDID (4 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do PERIMETRICS, INC's devices fall under?
Among its 7 most recently registered devices, the classes recorded for PERIMETRICS, INC's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from PERIMETRICS, INC in the registry?
The most recently registered devices listed for PERIMETRICS, INC include InnerView® System Base Station INV-2000, InnerView® System Handpiece INV-1000, InnerView® System Smart Tips INV-3000 and InnerView® System Disposable Tips INV-3000.