Valley Contax Single Vision (SV) Gas Permeable Contact Lens (roflufocon D, roflufocon E, tisilfocon A, hexafocon A, enflufocon A), Valley Contax Goldeneye Aspheric Front Multifocal (AFM) Gas Permeable Contact Lens (roflufocon D, roflufocon E, tisilfocon A, hexafocon A, enflufocon A), Valley Contax V Kone (VK) Gas Permeable Contact Lens (roflufocon D, roflufocon E, tisilfocon A, hexafocon A, enflufocon A)
K202860 is the FDA 510(k) clearance record for Valley Contax Single Vision (SV) Gas Permeable Contact Lens (roflufocon D, roflufocon E, tisilfocon A, hexafocon A, enflufocon A), Valley Contax Goldeneye Aspheric Front Multifocal (AFM) Gas Permeable Contact Lens (roflufocon D, roflufocon E, tisilfocon A, hexafocon A, enflufocon A), Valley Contax V Kone (VK) Gas Permeable Contact Lens (roflufocon D, roflufocon E, tisilfocon A, hexafocon A, enflufocon A), a class II device, cleared for Valley Contax, Inc. on under FDA product code HQD (Lens, Contact (Other Material) - Daily). FDA records list 3 510(k) clearances for Valley Contax, Inc., from to . As of , FDA records show no recalls naming K202860.
Clearance record
- Decision date
- Received
- (225 days to decision)
- Product code
- HQD Lens, Contact (Other Material) - Daily
- Regulation
- 21 CFR 886.5916
- Device class
- Class II
- Review panel
- Ophthalmic
- Applicant
- Valley Contax, Inc. 200 S. Mill St., Springfield OR
- 510(k) summary
- Summary PDF
- Third party review
- No
Clearances, product code HQD
Trailing 12 monthsShow the numbers
| Month | Clearances |
|---|---|
| November 2025 | 0 |
| December 2025 | 0 |
| January 2026 | 0 |
| February 2026 | 0 |
| March 2026 | 1 |
| April 2026 | 0 |
| May 2026 | 0 |
| June 2026 | 0 |
| July 2026 | 0 |
| August 2026 | 0 |
| September 2026 | 0 |
| October 2026 | 0 |
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