Contract manufacturerKWIK TEK, INC. (Denver, CO)ColoradoOphthalmicClass I
KWIK TEK, INC.
Contract manufacturer · Denver, CO
FDA-registered (openFDA, export of Oct 21, 2026) ISO 13485: not verified
- FDA registration
- 3000159466 (openFDA record; or search FDA's registration database)
- FEI number
- 3000159466
- Registered for
- FDA registration year 2026
- Establishment types
- Contract manufacturer
- Owner or operator
- AQUA LEISURE RECREATION LLC (FDA owner/operator no. 1221480)
- Registered address
- 12000 E 45th Ave, Denver, CO 80239
- Contract listings
- 2 device listings, 2 product codes, first listed Oct 20, 2005
- 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 |
|---|---|---|---|---|---|
| HOY | Shield, Eye, Ophthalmic (Including Sunlamp Protective Eyewear And Post-Mydriatic Eyewear) | Class I | Ophthalmic | Contract manufacturing | Oct 20, 2005 |
| HQY | Sunglasses (Non-Prescription Including Photosensitive) | Class I | Ophthalmic | Contract manufacturing | Jan 14, 2022 |