510(K) CLEARANCES 51 ▲2RECALLS POSTED 25 ▲2CLASS I 1PMA DECISIONS 50 ▲13WEEK ENDING / FDA DATA AS OF
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K093932Substantially Equivalent

Ethicon Physiomesh, Flexible Composite Mesh

Ethicon, Inc, Sommerville NJ / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K093932 is the FDA 510(k) clearance record for ETHICON PHYSIOMESH, FLEXIBLE COMPOSITE MESH, a class II device, cleared for Ethicon GmbH on under FDA product code FTL (Mesh, Surgical, Polymeric). FDA records list 208 510(k) clearances for Ethicon GmbH, from to . As of , FDA records show no recalls naming K093932.

Clearance record

Decision date
Received
(108 days to decision)
Product code
FTL Mesh, Surgical, Polymeric
Regulation
21 CFR 878.3300
Device class
Class II
Review panel
General, Plastic Surgery
Applicant
Ethicon GmbH Rt. 22 W. P.O. Box 151, Sommerville NJ
510(k) summary
Summary PDF
Third party review
No

Clearances, product code FTL

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