510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
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K162461Substantially Equivalent

Endoform Plastics and Reconstructive Matrix

Aroa Biosurgery (Formerly Mesynthes Limited), Auckland, NZ / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K162461 is the FDA 510(k) clearance record for Endoform Plastics and Reconstructive Matrix, a class II device, cleared for Aroa Biosurgery (Formerly Mesynthes Limited) on under FDA product code FTM (Mesh, Surgical). FDA records list one 510(k) clearance for Aroa Biosurgery (Formerly Mesynthes Limited). As of , FDA records show no recalls naming K162461.

Clearance record

Decision date
Received
(109 days to decision)
Product code
FTM Mesh, Surgical
Regulation
21 CFR 878.3300
Device class
Class II
Review panel
General, Plastic Surgery
Applicant
Aroa Biosurgery (Formerly Mesynthes Limited) 2 Kingsford Smith Pl., Airport Oaks, Auckland, NZ
510(k) summary
Summary PDF
Third party review
No

Clearances, product code FTM

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