Contract manufacturerDREVE AMERICA CORP. (Eden Prairie, MN)MinnesotaEar, nose and throatClass I
DREVE AMERICA CORP.
Contract manufacturer ยท Eden Prairie, MN
FDA-registered (openFDA, export of Oct 21, 2026) ISO 13485: not verified
- FDA registration
- 3007277229 (openFDA record; or search FDA's registration database)
- FEI number
- 3007277229
- Registered for
- FDA registration year 2026
- Establishment types
- Manufacturer; Contract manufacturer; Repackager or relabeler
- Owner or operator
- Dreve America Corp. (FDA owner/operator no. 10028157)
- Registered address
- 6477 City West Pkwy, Eden Prairie, MN 55344
- Contract listings
- 1 device listings, 1 product codes, first listed Nov 6, 2009
- 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 |
|---|---|---|---|---|---|
| ESD | Hearing Aid, Air-Conduction, Prescription | Class I | Ear, nose and throat | Contract manufacturing | Nov 6, 2009 |