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Xenmatrix 1152530

by Davol Inc.

Xenmatrix 1152530 is a Class II device made by Davol Inc., listed in FDA GUDID since 8 Mar 2017 (UDI-DI 00801741129018), registry data as of 22 Oct 2026.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Source GUDID, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00801741129018 UDI-DI Date8 Mar 2017ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name
Xenmatrix
Generic name
Extra-gynaecological surgical mesh, collagen, bioabsorbable, antimicrobial
Model / Ref / Catalog
1152530
Primary DI / UDI-DI
00801741129018
FDA product code
FTM, OXH, PIJ
GMDN term
Extra-gynaecological surgical mesh, collagen, bioabsorbable, antimicrobial
Device class
Class II
Regulation number
878.3300
GUDID distribution status
In Commercial Distribution
Size
Width — 30 Centimeter
Length — 25 Centimeter

Related devices

Category: Extra-gynaecological surgical mesh, collagen, bioabsorbable, antimicrobial

Similar devices

Other devices filed under FDA product code FTM (Mesh, surgical).

Other devices from Davol Inc.

See all devices from Davol Inc. →

Properties

  • Supplied sterile
  • Single use
  • Implantable
  • Prescription use
  • Combination product
  • Lot / batch number
  • Expiration date
Other properties (8, all answered No)