Contract manufacturerCLER VISION INC. (Riverside, CA)CaliforniaOphthalmicClass IIClass III
CLER VISION INC.
Contract manufacturer · Riverside, CA
FDA-registered (openFDA, export of Oct 21, 2026) ISO 13485: not verified
- FDA registration
- 3022988037 (openFDA record; or search FDA's registration database)
- FEI number
- 3022988037
- Registered for
- FDA registration year 2026
- Establishment types
- Contract manufacturer
- Owner or operator
- Cler Vision Inc. (FDA owner/operator no. 10094772)
- Registered address
- 7338 Sycamore Canyon Blvd, Unit 2, Riverside, CA 92508
- Contract listings
- 7 device listings, 3 product codes, first listed Dec 22, 2025
- 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 |
|---|---|---|---|---|---|
| HQD | Lens, Contact (Other Material) - Daily | Class II | Ophthalmic | Contract manufacturing | Dec 22, 2025 |
| MUW | Lens, Contact (Orthokeratology) | Class II | Ophthalmic | Contract manufacturing | Dec 22, 2025 |
| NUU | Lens, Contact, Orthokeratology, Overnight | Class III | Ophthalmic | Contract manufacturing | Apr 27, 2026 |