510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
K832762Substantially Equivalent

Miller/nadler Glare Tester

Titmus Optical, Inc., Walker MI / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K832762 is the FDA 510(k) clearance record for MILLER/NADLER GLARE TESTER, a class II device, cleared for Titmus Optical, Inc. on under FDA product code HLX (Photostimulator, Ac-Powered). FDA records list 3 510(k) clearances for Titmus Optical, Inc., from to . As of , FDA records show no recalls naming K832762.

Clearance record

Decision date
Received
(44 days to decision)
Product code
HLX Photostimulator, Ac-Powered
Regulation
21 CFR 886.1630
Device class
Class II
Review panel
Ophthalmic
Applicant
Titmus Optical, Inc. 4221 Richmond Rd., NW, Walker MI
Third party review
No

Clearances, product code HLX

Trailing 12 months

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

FDA records show no clearances under product code HLX in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code HLX, 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