Contract manufacturerMIDWEST INTERVENTIONAL SYSTEMS (Maple Grove, MN)MinnesotaOrthopedicEar, nose and throatCardiovascularClass IIClass I
MIDWEST INTERVENTIONAL SYSTEMS
Contract manufacturer ยท Maple Grove, MN
FDA-registered (openFDA, export of Oct 21, 2026) ISO 13485: not verified
- FDA registration
- 3016842760 (openFDA record; or search FDA's registration database)
- FEI number
- 3016842760
- Registered for
- FDA registration year 2026
- Establishment types
- Contract manufacturer
- Owner or operator
- Midwest Interventional Systems (FDA owner/operator no. 10073120)
- Registered address
- 6450 Wedgwood Rd N, STE 110, Maple Grove, MN 55311
- Contract listings
- 4 device listings, 5 product codes, first listed Jul 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 |
|---|---|---|---|---|---|
| HRX | Arthroscope | Class II | Orthopedic | Contract manufacturing | Dec 12, 2025 |
| LRC | Instrument, Ent Manual Surgical | Class I | Ear, nose and throat | Contract manufacturing | Jul 21, 2023 |
| MJN | Catheter, Intravascular Occluding, Temporary | Class II | Cardiovascular | Contract manufacturing | Feb 23, 2024 |
| NDN | Cement, Bone, Vertebroplasty | Class II | Orthopedic | Contract manufacturing | Dec 12, 2025 |
| PNZ | Eustachian Tube Balloon Dilation Device | Class II | Ear, nose and throat | Contract manufacturing | Jul 21, 2023 |