Product code KYE— Ophthalmic
CONTACT LENS REMOVER AND INSERTER
- Classification name
- Inserter/Remover Contact Lens
- Device class
- Class 1
- Regulation
- 21 CFR 886.5420
- Advisory panel
- Ophthalmic
- Total cleared
- 12
- First cleared
- Most recent
Market context for product code KYE
FDA has cleared devices under product code KYE between 1978 and 1987, filed by 8 applicant companies. No FDA device recalls reference this product code. Class I devices are low-risk and subject to FDA general controls; many Class I device types are exempt from 510(k) premarket notification.
Clearances per year
- 1987
- 1985
- 1983
- 1979
- 1978
Top applicants under product code KYE
Recent clearances under product code KYE
- K872567 — SOFT CONTACT LENS REMOVER
- K872591 — HARD CONTACT LENS REMOVER. ITEM #289
- K871130 — CONTACT LENS TWEEZERS
- K870072 — SUMMIT OPTICS CONTACT LENS REMOVER
- K850983 — MARLIN SOFT LENS TWEEZER
- K850984 — MARLIN SOFT LENS HANDLER
- K830738 — LENSERT CONTACT LENS CLEANING & INSERT
- K830496 — DMV ANGLER
- K782140 — REMOVER, SOFT-SERT CONTACT LENS
- K780931 — SOFT LENS INSERTER
- K780663 — CONTACT LENS REMOVER AND INSERTER
- K780664 — SOFT LENS REMOVER/INSERTER/MANIPULATOR
Data sourced from openFDA. This site is unofficial and independent of the FDA.