Contract manufacturerCovidien llc (Plymouth, MN)MinnesotaGeneral and plastic surgeryClass II
Covidien llc
Contract manufacturer · Plymouth, MN
FDA-registered (openFDA, export of Oct 21, 2026) ISO 13485: not verified
- FDA registration
- 3004962788 (openFDA record; or search FDA's registration database)
- FEI number
- 3004962788
- Registered for
- FDA registration year 2026
- Establishment types
- Complaint file establishment; Specification developer; Manufacturer for export only; Manufacturer; Contract manufacturer; Repackager or relabeler
- Owner or operator
- Covidien llc (FDA owner/operator no. 1282497)
- Registered address
- 161 CHESHIRE LANE, SUITE 100, Plymouth, MN 55441
- Contract listings
- 1 device listings, 1 product codes, first listed May 16, 2014
- 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 |
|---|---|---|---|---|---|
| NEY | System, Ablation, Microwave And Accessories | Class II | General and plastic surgery | Contract manufacturing | May 16, 2014 |