Contract manufacturerMME Willow Lake (Vadnais Hts, MN)MinnesotaAnesthesiologyCardiovascularGeneral and plastic surgeryOphthalmicClass IClass II
MME Willow Lake
Contract manufacturer ยท Vadnais Hts, MN
FDA-registered (openFDA, export of Oct 21, 2026) ISO 13485: not verified
- FDA registration
- 3017056829 (openFDA record; or search FDA's registration database)
- FEI number
- 3017056829
- Registered for
- FDA registration year 2026
- Establishment types
- Contract manufacturer
- Owner or operator
- MME Group (A Seaway Plastics Engineering Company) (FDA owner/operator no. 10051967)
- Registered address
- 1185 Willow Lake Blvd., Vadnais Hts, MN 55110
- Contract listings
- 4 device listings, 4 product codes, first listed Apr 24, 2018
- 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 |
|---|---|---|---|---|---|
| CBH | Device, Fixation, Tracheal Tube | Class I | Anesthesiology | Contract manufacturing | Nov 25, 2025 |
| DXC | Clamp, Vascular | Class II | Cardiovascular | Contract manufacturing | Nov 25, 2025 |
| GEY | Motor, Surgical Instrument, Ac-Powered | Class I | General and plastic surgery | Contract manufacturing | Apr 4, 2026 |
| ORZ | Eyelid Thermal Pulsation System | Class II | Ophthalmic | Contract manufacturing | Apr 24, 2018 |