510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K872747Substantially Equivalent

Laser Centering Device

Innomed, Inc., Brea CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K872747 is the FDA 510(k) clearance record for LASER CENTERING DEVICE, a class I device, cleared for Innomed Corp. on under FDA product code HMR (Marker, Ocular). FDA records list 3 510(k) clearances for Innomed Corp., from to . As of , FDA records show no recalls naming K872747.

Clearance record

Decision date
Received
(53 days to decision)
Product code
HMR Marker, Ocular
Regulation
21 CFR 886.4570
Device class
Class I
Review panel
Ophthalmic
Applicant
Innomed Corp. 620 Lunar, Brea CA
Third party review
No

Clearances, product code HMR

Trailing 12 months

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

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