SharpMed, LLC
United Statesfrom the FDA registration address FDA FEI 3017828726
- Devices
- 2
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
- Registry: GUDID
- Registry: GUDID
Company details
- FDA FEI number
- 3017828726
- DUNS number
- 964850080
- Address
- 14362 N Frank Lloyd Wright Blvd Ste 1000, Scottsdale, AZ, 85260
Frequently asked questions
How many devices does SharpMed, LLC have in the registry?
The registry currently lists 2 devices for SharpMed, LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list SharpMed, LLC's devices?
Among its 2 most recently registered devices, SharpMed, LLC has devices listed in FDA GUDID (2 devices).
What risk classes do SharpMed, LLC's devices fall under?
Among its 2 most recently registered devices, the classes recorded for SharpMed, LLC's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from SharpMed, LLC in the registry?
The most recently registered devices listed for SharpMed, LLC include Turbo O2 Convenience Kit 100-60-0100 and Turbo O2 Cap 100-60-0098.