510(K) CLEARANCES 67 ▼8RECALLS POSTED 26CLASS I 2PMA DECISIONS 40 ▼14WEEK ENDING / FDA DATA AS OF
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K895741Substantially Equivalent

Clas Photokeratoscope

Kera-Metrics Corp., San Diego CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K895741 is the FDA 510(k) clearance record for CLAS PHOTOKERATOSCOPE, a class I device, cleared for Kera-Metrics Corp. on under FDA product code HLQ (Keratoscope, Ac-Powered). FDA records list one 510(k) clearance for Kera-Metrics Corp. As of , FDA records show no recalls naming K895741.

Clearance record

Decision date
Received
(288 days to decision)
Product code
HLQ Keratoscope, Ac-Powered
Regulation
21 CFR 886.1350
Device class
Class I
Review panel
Ophthalmic
Applicant
Kera-Metrics Corp. 11211 Sorrento Valley Rd.,, San Diego CA
Third party review
No

Clearances, product code HLQ

Trailing 12 months

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

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