510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K862517Substantially Equivalent

Bausch & Lomb Contact Lens Viewer

Bausch & Lomb Incorporated, Rochester NY / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K862517 is the FDA 510(k) clearance record for BAUSCH & LOMB CONTACT LENS VIEWER, a class I device, cleared for Bausch & Lomb, Inc. on under FDA product code HLF (Device, Measuring, Lens Radius, Ophthalmic). FDA records list 131 510(k) clearances for Bausch & Lomb Incorporated, from to . As of , FDA records show no recalls naming K862517.

Clearance record

Decision date
Received
(41 days to decision)
Product code
HLF Device, Measuring, Lens Radius, Ophthalmic
Regulation
21 CFR 886.1430
Device class
Class I
Review panel
Ophthalmic
Applicant
Bausch & Lomb, Inc. 1400 N. Goodman St., Rochester NY
Third party review
No

Clearances, product code HLF

Trailing 12 months

FDA records hold no clearances under product code HLF in the trailing twelve months.

FDA records show no clearances under product code HLF in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code HLF, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260