Psoria-Shield Inc
United Statesfrom the FDA registration address FDA establishment FEI 3008872264
- Devices
- 4
- Registrations
- FDA
- FDA recalls
- 0
What Psoria-Shield Inc makes
Psoria-Shield Inc manufactures professional ultraviolet phototherapy units designed for medical treatment, including the Enhanced AURORA™ Medical Diode System and associated accessories. These devices are intended for controlled light therapy to manage skin conditions like psoriasis.
The company’s ultraviolet phototherapy units fall under FDA Class II regulation and are listed in the FDA’s Unique Device Identifier (UDI) database. The manufacturer is based in the United States.
Catalogue
- Registry: GUDID
Psoria-Shield AURORA Ref K192411
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Psoria-Light Ref K103540
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3008872264
- Address
- 409 Mandeville St, Utica, NY, 13502
Frequently asked questions
How many devices does PSORIA-SHIELD INC have in the registry?
The registry currently lists 4 devices for PSORIA-SHIELD INC. Devices recorded under merged duplicate company entries are counted once.
Which registries list PSORIA-SHIELD INC's devices?
Among its 4 most recently registered devices, PSORIA-SHIELD INC has devices listed in FDA 510(k) (3 devices) and FDA GUDID (1 device). A device can be listed in more than one registry, so these counts overlap.
What risk classes do PSORIA-SHIELD INC's devices fall under?
Among its 4 most recently registered devices, the classes recorded for PSORIA-SHIELD INC's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from PSORIA-SHIELD INC in the registry?
The most recently registered devices listed for PSORIA-SHIELD INC include Enhanced AURORA™ Medical Diode System, and related accessories 2000, Psoria-Shield AURORA, Enhanced AURORA™ Medical Diode System, and related accessories and PSORIA-LIGHT.