Atlas FDA

KYE

12 FDA 510(k) clearances · Product code

42 daysmedian time to decision
183 days90th percentile
12clearances measured

FDA profile

Official device name
Inserter/Remover Contact Lens
Device class
Class I (low risk)
Regulation
21 CFR 886.5420
Medical specialty
Ophthalmic
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RecordFirmDate
SOFT CONTACT LENS REMOVER (K872567)Magnivision, Inc.1987-08-10
HARD CONTACT LENS REMOVER. ITEM #289 (K872591)Magnivision, Inc.1987-08-04
CONTACT LENS TWEEZERS (K871130)S. M. C. Medi-Tech Corp.1987-05-12
SUMMIT OPTICS CONTACT LENS REMOVER (K870072)Dayton Mfg. Co.1987-02-12
MARLIN SOFT LENS HANDLER (K850984)Marlin Industries1985-09-10
MARLIN SOFT LENS TWEEZER (K850983)Marlin Industries1985-09-10
LENSERT CONTACT LENS CLEANING & INSERT (K830738)Jermyn Specialties of California1983-06-10
DMV ANGLER (K830496)Dmv Contact Lens Co.1983-03-09
REMOVER, SOFT-SERT CONTACT LENS (K782140)Mcmurray and Pendergost1979-02-12
SOFT LENS INSERTER (K780931)Soft-Sert1978-06-28
SOFT LENS REMOVER/INSERTER/MANIPULATOR (K780664)Dmv Contact Lens Co.1978-05-17
CONTACT LENS REMOVER AND INSERTER (K780663)Dmv Contact Lens Co.1978-05-17

Track KYE automatically

Every clearance here is in the API, with alerts when new ones post.