# Trelleborg Sealing Solutions Us, Inc. (contract manufacturer, Paso Robles, CA): 3 new FDA device listings, incl. implant, eye valve

**Score:** 80/100

| Field | Value |
|---|---|
| Establishment | Trelleborg Sealing Solutions Us, Inc. |
| Owner / operator | Trelleborg Sealing Solutions US, Inc. |
| Role | Contract manufacturer |
| Establishment types | Manufacture Medical Device for Another Party (Contract Manufacturer) |
| Location | Paso Robles, CA, US |
| New listings | 3 |
| Devices | Implant, Eye Valve; Splint, Intranasal Septal; Implantable Cardioverter Defibrillator (Non-Crt) |
| Product codes | KYF, LYA, LWS |
| Device classes | Class I, Class II, Class III |
| Medical specialties | Ophthalmic, Ear, Nose, Throat |
| First new listing | 2026-06-17 |
| Latest new listing | 2026-06-17 |
| FDA registration number | 3013674629 |
| Registration expires | 2026-12-31 |

## Why this score
- Contract manufacturer or sterilizer adding work.
- Class II or III devices: QMS and regulatory demands.
- Several new listings at once.
- U.S. establishment.

Source: openFDA device registration and listing endpoint (U.S. Food and Drug Administration) (https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm). Last refreshed: 2026-10-28T20:51:27.468Z.
From the openFDA device registration and listing data, refreshed weekly. A listing shows a device an establishment says it makes or handles for the U.S. market; it is not FDA clearance or approval. Contact persons and street addresses are not stored. Verify in the FDA Establishment Registration and Device Listing database.