Contract manufacturerMINNESOTA MEDTEC, INC. (Maple Grove, MN)MinnesotaGastroenterology and urologyCardiovascularClass II
MINNESOTA MEDTEC, INC.
Contract manufacturer ยท Maple Grove, MN
FDA-registered (openFDA, export of Oct 21, 2026) ISO 13485: not verified
- FDA registration
- 2134626 (openFDA record; or search FDA's registration database)
- FEI number
- 3003007911
- Registered for
- FDA registration year 2026
- Establishment types
- Manufacturer for export only; Contract manufacturer
- Owner or operator
- MINNESOTA MEDTEC, INC. (FDA owner/operator no. 9036710)
- Registered address
- 11760 Justen Circle, Mail drop Unit B, Maple Grove, MN 55369
- Contract listings
- 2 device listings, 2 product codes, first listed Dec 21, 2023
- 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 |
|---|---|---|---|---|---|
| KLA | Monitor, Esophageal Motility, Anorectal Motility, And Tube | Class II | Gastroenterology and urology | Contract manufacturing | Aug 11, 2025 |
| LIT | Catheter, Angioplasty, Peripheral, Transluminal | Class II | Cardiovascular | Contract manufacturing | Dec 21, 2023 |