510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K062341Substantially Equivalent

Male Remeex System

Specialities Remeex International, S.L., Minneapolis MN / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K062341 is the FDA 510(k) clearance record for MALE REMEEX SYSTEM, a class II device, cleared for Specialities Remeex International, S.L. on under FDA product code OTM (Mesh, Surgical, For Stress Urinary Incontinence, Male). FDA's definition for product code OTM reads: "surgical treatment of male stress urinary incontinence post-prostatectomy". FDA records list 3 510(k) clearances for Specialities Remeex International, S.L., from to . As of , FDA records show no recalls naming K062341.

Clearance record

Decision date
Received
(84 days to decision)
Product code
OTM Mesh, Surgical, For Stress Urinary Incontinence, Male
Regulation
21 CFR 878.3300
Device class
Class II
Review panel
General, Plastic Surgery
Applicant
Specialities Remeex International, S.L. 7307 Glouchester Dr., Minneapolis MN
510(k) summary
Summary PDF
Third party review
No

Clearances, product code OTM

Trailing 12 months

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

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