510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K111121Substantially Equivalent

Vitamesh (Tm) Blue Lightweight Macroporous Pp Surgical Mesh

Proxy Biomedical Ltd., Stillwater MN / Special, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K111121 is the FDA 510(k) clearance record for VITAMESH (TM) BLUE LIGHTWEIGHT MACROPOROUS PP SURGICAL MESH, a class II device, cleared for Proxy Biomedical , Ltd. on under FDA product code FTL (Mesh, Surgical, Polymeric). FDA records list 6 510(k) clearances for Proxy Biomedical , Ltd., from to . As of , FDA records show no recalls naming K111121.

Clearance record

Decision date
Received
(22 days to decision)
Product code
FTL Mesh, Surgical, Polymeric
Regulation
21 CFR 878.3300
Device class
Class II
Review panel
General, Plastic Surgery
Applicant
Proxy Biomedical , Ltd. P.O. Box 560, Stillwater MN
510(k) summary
Summary PDF
Third party review
No

Clearances, product code FTL

Trailing 12 months
1 clearance under product code FTL in the twelve months to October 2026, May 2026 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code FTL, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20261
June 20260
July 20260
August 20260
September 20260
October 20260