510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K923843Substantially Equivalent

Fogless

Sorex Medical, Salt Lake City UT / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K923843 is the FDA 510(k) clearance record for FOGLESS, a class II device, cleared for Sorex Medical on under FDA product code OCT (Anti Fog Solution And Accessories, Endoscopy). FDA's definition for product code OCT reads: "To prevent, reduce or eliminate condensation (fog) on endoscopic lens". FDA records list 9 510(k) clearances for Sorex Medical, from to . As of , FDA records show no recalls naming K923843.

Clearance record

Decision date
Received
(602 days to decision)
Product code
OCT Anti Fog Solution And Accessories, Endoscopy
Regulation
21 CFR 876.1500
Device class
Class II
Review panel
Gastroenterology, Urology
Applicant
Sorex Medical 5725 W. Harold Gatty Dr., Salt Lake City UT
510(k) summary
Statement
Third party review
No

Clearances, product code OCT

Trailing 12 months

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

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