510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K792273Substantially Equivalent

Dexide Dis. Prep Sponge W/idex Patient P

Dexide, Inc., Mchenry IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K792273 is the FDA 510(k) clearance record for DEXIDE DIS. PREP SPONGE W/IDEX PATIENT P, a class I device, cleared for Dexide, Inc. on under FDA product code GEC (Brush, Scrub, Operating-Room). FDA records list 38 510(k) clearances for Dexide, Inc., from to . As of , FDA records show no recalls naming K792273.

Clearance record

Decision date
Received
(27 days to decision)
Product code
GEC Brush, Scrub, Operating-Room
Regulation
21 CFR 878.4800
Device class
Class I
Review panel
General, Plastic Surgery
Applicant
Dexide, Inc. 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code GEC

Trailing 12 months

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

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