Novidan, Inc.
United Statesfrom the FDA registration address FDA FEI 3015651976
- Devices
- 49
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
Catalogue
Search and filter all 49 devicesCompany details
- FDA FEI number
- 3015651976
- DUNS number
- 117003805
- Address
- 678 Mendelssohn Ave N, Golden Valley, MN, 55427
- [email protected]
- Phone
- 833-668-4326
Frequently asked questions
How many devices does Novidan, Inc. have in the registry?
The registry currently lists 49 devices for Novidan, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Novidan, Inc.'s devices?
Among its 49 most recently registered devices, Novidan, Inc. has devices listed in FDA GUDID (49 devices).
What risk classes do Novidan, Inc.'s devices fall under?
Among its 49 most recently registered devices, the classes recorded for Novidan, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Novidan, Inc. in the registry?
The most recently registered devices listed for Novidan, Inc. include Sonify Hearing 99-0016-02, Novidan 99-0010-05, NoviMed Hearing 99-0019-03 and Novidan 99-0002-23.