510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K960522Substantially Equivalent

Diopexy Probe

Iriderm Div., Mountain View CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K960522 is the FDA 510(k) clearance record for DIOPEXY PROBE, a class II device, cleared for Iriderm Div. on under FDA product code HQF (Laser, Ophthalmic). FDA records list 10 510(k) clearances for Iriderm Div., from to . As of , FDA records show no recalls naming K960522.

Clearance record

Decision date
Received
(164 days to decision)
Product code
HQF Laser, Ophthalmic
Regulation
21 CFR 886.4390
Device class
Class II
Review panel
Ophthalmic
Applicant
Iriderm Div. 340 Pioneer Way, Mountain View CA
510(k) summary
Summary
Third party review
No

Clearances, product code HQF

Trailing 12 months
2 clearances under product code HQF in the twelve months to October 2026, February 2026 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code HQF, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20261
March 20260
April 20261
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260