510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K900138Substantially Equivalent

Motech Titanium Surgical Mesh

Biedermann Motech GmbH, Olney MD / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K900138 is the FDA 510(k) clearance record for MOTECH TITANIUM SURGICAL MESH, a class II device, cleared for Biedermann Motech GmbH on under FDA product code EZX (Mesh, Surgical, Metal). FDA records list 2 510(k) clearances for Biedermann Motech GmbH, from to . As of , FDA records show no recalls naming K900138.

Clearance record

Decision date
Received
(68 days to decision)
Product code
EZX Mesh, Surgical, Metal
Regulation
21 CFR 878.3300
Device class
Class II
Review panel
General, Plastic Surgery
Applicant
Biedermann Motech GmbH 18159 Village Mart Dr., Olney MD
Third party review
No

Clearances, product code EZX

Trailing 12 months

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

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