Neuspera Medical, Inc.
United Statesfrom the FDA registration address FDA establishment FEI 3014845032
- Devices
- 52
- Registrations
- FDA
- FDA recalls
- 0
Catalogue
Search and filter all 52 devicesShowing 1-50 of 52
Company details
- FDA FEI number
- 3014845032
- Address
- 51 Daggett Dr, San Jose, CA, 95134
Frequently asked questions
How many devices does NEUSPERA MEDICAL, INC. have in the registry?
The registry currently lists 52 devices for NEUSPERA MEDICAL, INC.. Devices recorded under merged duplicate company entries are counted once.
Which registries list NEUSPERA MEDICAL, INC.'s devices?
Among its 50 most recently registered devices, NEUSPERA MEDICAL, INC. has devices listed in FDA 510(k) (1 device) and FDA GUDID (49 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do NEUSPERA MEDICAL, INC.'s devices fall under?
Among its 50 most recently registered devices, the classes recorded for NEUSPERA MEDICAL, INC.'s devices are Class II and Class III. Each device page shows its own class and authorisation.
What are the newest devices from NEUSPERA MEDICAL, INC. in the registry?
The most recently registered devices listed for NEUSPERA MEDICAL, INC. include Neuspera SNM System SNS-28, Neuspera SNM System ESK-1, Neuspera SNM System PAK-1 and Neuspera SNM System WU-L-XS.