Acuity 18 (enflufocon A) Rigid Gas Permeable Contact Lens, Acuity 58 (enflufocon B) Rigid Gas Permeable Contact Lens, Acuity 85 (Oprifocon A) Rigid Gas Permeable Contact Lens, Acuity 100 (hexafocon A) Rigid Gas Permeable Contact Lens
K180988 is the FDA 510(k) clearance record for Acuity 18 (enflufocon A) Rigid Gas Permeable Contact Lens, Acuity 58 (enflufocon B) Rigid Gas Permeable Contact Lens, Acuity 85 (Oprifocon A) Rigid Gas Permeable Contact Lens, Acuity 100 (hexafocon A) Rigid Gas Permeable Contact Lens, a class II device, cleared for Acuity Polymers, Inc. on under FDA product code HQD (Lens, Contact (Other Material) - Daily). FDA records list 11 510(k) clearances for Acuity Polymers, Inc., from to . As of , FDA records show no recalls naming K180988.
Clearance record
- Decision date
- Received
- (53 days to decision)
- Product code
- HQD Lens, Contact (Other Material) - Daily
- Regulation
- 21 CFR 886.5916
- Device class
- Class II
- Review panel
- Ophthalmic
- Applicant
- Acuity Polymers, Inc. 1667 Lake Ave.,, Rochester NY
- 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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