Perioview, LLC
Also registered as Perioview, Inc.
United Statesfrom the FDA registration address FDA establishment FEI 3027060896
- Devices
- 1
- Registrations
- FDA
- FDA recalls
- 0
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Jacobyscope Ref K953912
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3027060896
- Address
- 12425 W Bell Rd Ste C110, Surprise, AZ, 85378
Frequently asked questions
How many devices does PERIOVIEW, LLC have in the registry?
The registry currently lists 1 device for PERIOVIEW, LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list PERIOVIEW, LLC's devices?
Among its 1 most recently registered device, PERIOVIEW, LLC has devices listed in FDA 510(k) (1 device).
What risk classes do PERIOVIEW, LLC's devices fall under?
Among its 1 most recently registered device, the classes recorded for PERIOVIEW, LLC's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from PERIOVIEW, LLC in the registry?
The most recently registered devices listed for PERIOVIEW, LLC include JACOBYSCOPE.