510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K871313Substantially Equivalent

Ultra-Fresh Deodorant

Mentor, Minneapolis MN / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K871313 is the FDA 510(k) clearance record for ULTRA-FRESH DEODORANT, a class I device, cleared for Mentor Corp. on under FDA product code GDS (Bag, Stomal). FDA records list 65 510(k) clearances for Mentor Corp., from to . As of , FDA records show no recalls naming K871313.

Clearance record

Decision date
Received
(336 days to decision)
Product code
GDS Bag, Stomal
Regulation
21 CFR 876.5900
Device class
Class I
Review panel
Gastroenterology, Urology
Applicant
Mentor Corp. 2700 Fwy. Blvd., Minneapolis MN
Third party review
No

Clearances, product code GDS

Trailing 12 months

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

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