510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K781507Substantially Equivalent

Retinometer

Coburn Optical Ind., Inc., Mchenry IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K781507 is the FDA 510(k) clearance record for RETINOMETER, a class II device, cleared for Coburn Optical Ind., Inc. on under FDA product code HPJ (Instrument, Visual Field, Laser). FDA records list 14 510(k) clearances for Coburn Optical Ind., Inc., from to . As of , FDA records show no recalls naming K781507.

Clearance record

Decision date
Received
(75 days to decision)
Product code
HPJ Instrument, Visual Field, Laser
Regulation
21 CFR 886.1360
Device class
Class II
Review panel
Ophthalmic
Applicant
Coburn Optical Ind., Inc. 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code HPJ

Trailing 12 months

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

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