Contract manufacturerNOVIDAN, INC. (Golden Valley, MN)MinnesotaEar, nose and throatClass II
NOVIDAN, INC.
Contract manufacturer ยท Golden Valley, MN
FDA-registered (openFDA, export of Oct 21, 2026) ISO 13485: not verified
- FDA registration
- 3015651976 (openFDA record; or search FDA's registration database)
- FEI number
- 3015651976
- Registered for
- FDA registration year 2026
- Establishment types
- Complaint file establishment; Manufacturer; Contract manufacturer
- Owner or operator
- Novidan, Inc. (FDA owner/operator no. 10061834)
- Registered address
- 678 Mendelssohn Ave N, Golden Valley, MN 55427
- Contract listings
- 2 device listings, 3 product codes, first listed May 12, 2021
- Certification
- Not verified. We have no certification data for this facility yet.
Devices listed as contract work
Each row is an FDA product code this facility lists under its contract establishment type, with the date of its earliest such listing.
| Product code | Device (FDA name) | Class | Category | Role | First listed |
|---|---|---|---|---|---|
| QDD | Self-Fitting Air-Conduction Hearing Aid, Prescription | Class II | Ear, nose and throat | Contract manufacturing | May 12, 2021 |
| QUG | Hearing Aid, Air-Conduction With Wireless Technology, Over The Counter | Class II | Ear, nose and throat | Contract manufacturing | Dec 2, 2022 |
| QUH | Self-Fitting Air-Conduction Hearing Aid, Over The Counter | Class II | Ear, nose and throat | Contract manufacturing | May 12, 2021 |