510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K062758Substantially Equivalent

Owl Urf-3Ap

Diros Technology, Inc., Markham, Ontario, CA / Special, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K062758 is the FDA 510(k) clearance record for OWL URF-3AP, a class II device, cleared for Diros Technology, Inc. on under FDA product code GXD (Generator, Lesion, Radiofrequency). FDA records list 8 510(k) clearances for Diros Technology, Inc., from to . As of , FDA records show no recalls naming K062758.

Clearance record

Decision date
Received
(12 days to decision)
Product code
GXD Generator, Lesion, Radiofrequency
Regulation
21 CFR 882.4400
Device class
Class II
Review panel
Neurology
Applicant
Diros Technology, Inc. 232 Hood Rd., Markham, Ontario, CA
510(k) summary
Summary PDF
Third party review
No

Clearances, product code GXD

Trailing 12 months

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

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