Sovereign America
Country not established
- Devices
- 3
What Sovereign America makes
The company produces single-use, non-antimicrobial surgical and medical face masks designed for clinical and procedural use. These masks are intended for one-time application to reduce the risk of cross-contamination in healthcare settings.
The product portfolio is classified under FDA’s Class II regulatory category and is listed in the FDA’s Unique Device Identifier (UDI) database. The company operates from the United States.
Catalogue
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
Company details
- DUNS number
- 626525463
- [email protected]
- Phone
- 256-734-3937
Frequently asked questions
How many devices does Sovereign America have in the registry?
The registry currently lists 3 devices for Sovereign America. Devices recorded under merged duplicate company entries are counted once.
Which registries list Sovereign America's devices?
Among its 3 most recently registered devices, Sovereign America has devices listed in FDA GUDID (3 devices).
What risk classes do Sovereign America's devices fall under?
Among its 3 most recently registered devices, the classes recorded for Sovereign America's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Sovereign America in the registry?
The most recently registered devices listed for Sovereign America include Sovereign America 2000SM1, Sovereign America 2000SM3 and Sovereign America 2000SM2.