Contract manufacturerTrelleborg Sealing Solutions Litchfield (Litchfield, MN)MinnesotaOrthopedicNeurologyClass II
Trelleborg Sealing Solutions Litchfield
Contract manufacturer · Litchfield, MN
FDA-registered (openFDA, export of Oct 21, 2026) ISO 13485: not verified
- FDA registration
- 3004126422 (openFDA record; or search FDA's registration database)
- FEI number
- 3004126422
- Registered for
- FDA registration year 2026
- Establishment types
- Contract manufacturer
- Owner or operator
- Trelleborg Sealing Solutions Plymouth LLC (FDA owner/operator no. 9102441)
- Registered address
- 45 N Precision Dr, Litchfield, MN 55355
- Contract listings
- 2 device listings, 3 product codes, first listed Feb 19, 2013
- 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 |
|---|---|---|---|---|---|
| KWL | Prosthesis, Hip, Hemi-, Femoral, Metal | Class II | Orthopedic | Contract manufacturing | Jan 14, 2020 |
| KWY | Prosthesis, Hip, Hemi-, Femoral, Metal/Polymer, Cemented Or Uncemented | Class II | Orthopedic | Contract manufacturing | Jan 14, 2020 |
| OLO | Orthopedic Stereotaxic Instrument | Class II | Neurology | Contract manufacturing | Feb 19, 2013 |