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IntePro Y-Mesh 72404000

by Endo Pharmaceuticals Inc. GUDID

Withdrawn United States

Overview

IntePro Y-Mesh is a medical device designed to treat vaginal pelvic organ prolapse (POP) through reinforcement and/or bridging of the supporting tissues of the pelvic floor. It consists of a sterile woven/knitted or porous synthetic polymer mesh, typically available with various material attributes.

Regulatory status

as of 28 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00814723020333 UDI-DIDate24 Oct 2015ListedStatusWithdrawn

Coverage

1 jurisdiction

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  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not known
  • Not covered

United States — GUDID listing Listed

Recalls

0 recalls · FDA

No FDA recalls on record, checked 22 Oct 2026.

Specification

GUDID

Trade Name
IntePro Y-Mesh
Generic Name
Pelvic organ prolapse surgical mesh, synthetic polymer
Model / Ref / Catalog
72404000
Primary DI / UDI-DI
00814723020333
FDA Product Code
OTO
GMDN Term
Pelvic organ prolapse surgical mesh, synthetic polymer
Device Class
Class II
Regulation Number
878.3300
Commercial Distribution
Not in Commercial Distribution

Other devices from Endo Pharmaceuticals Inc.

Properties

  • Sterile
  • Single Use
  • Implantable
  • Prescription Use
  • Lot / Batch Number
  • Expiration Date
  • Manufacturing Date

Other properties (7)

  • Contains Latex: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Serial Number: No