Contract manufacturerTrelleborg Sealing Solutions US, Inc. (Tustin, CA)CaliforniaOphthalmicCardiovascularEar, nose and throatClass IIClass IIIClass I
Trelleborg Sealing Solutions US, Inc.
Contract manufacturer ยท Tustin, CA
FDA-registered (openFDA, export of Oct 21, 2026) ISO 13485: not verified
- FDA registration
- 2022502 (openFDA record; or search FDA's registration database)
- FEI number
- 2022502
- Registered for
- FDA registration year 2026
- Establishment types
- Contract manufacturer
- Owner or operator
- Trelleborg Sealing Solutions US, Inc. (FDA owner/operator no. 2022502)
- Registered address
- 2761 Walnut Ave, Tustin, CA 92780
- Contract listings
- 3 device listings, 3 product codes, first listed Jan 13, 2017
- 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 |
|---|---|---|---|---|---|
| KYF | Implant, Eye Valve | Class II | Ophthalmic | Contract manufacturing | Jan 13, 2017 |
| LWS | Implantable Cardioverter Defibrillator (Non-Crt) | Class III | Cardiovascular | Contract manufacturing | Apr 18, 2022 |
| LYA | Splint, Intranasal Septal | Class I | Ear, nose and throat | Contract manufacturing | Oct 22, 2021 |