Universal Shapers
United Statesfrom the FDA registration address FDA establishment FEI 3042750929
- Devices
- 5
- Registrations
- FDA
- FDA recalls
- 0
Catalogue
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
Company details
- FDA FEI number
- 3042750929
- Address
- 94 Cypress Dr, Woodbury, NY, 11797
Frequently asked questions
How many devices does UNIVERSAL SHAPERS have in the registry?
The registry currently lists 5 devices for UNIVERSAL SHAPERS. Devices recorded under merged duplicate company entries are counted once.
Which registries list UNIVERSAL SHAPERS's devices?
Among its 5 most recently registered devices, UNIVERSAL SHAPERS has devices listed in FDA GUDID (5 devices).
What risk classes do UNIVERSAL SHAPERS's devices fall under?
Among its 5 most recently registered devices, the classes recorded for UNIVERSAL SHAPERS's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from UNIVERSAL SHAPERS in the registry?
The most recently registered devices listed for UNIVERSAL SHAPERS include Universal Shapers Cortical Release Drill CR 4.2mm X 5mm, Universal Shapers Cortical Release Drill CR 3.5mm X 5mm, Universal Shapers Scalloping Drill SS5 and Universal Shapers Scalloping Drill SS6.