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Strattice Reconstructive Tissue Matrix 1525002

by Lifecell Corp

Strattice Reconstructive Tissue Matrix 1525002 is a Class II device made by Lifecell Corp, listed in FDA GUDID since 17 Sep 2015 (UDI-DI M32815250020), registry data as of 23 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 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing NumberM32815250020 UDI-DI Date17 Sep 2015ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade name
Strattice Reconstructive Tissue Matrix
Generic name
Extra-gynaecological surgical mesh, collagen, bioabsorbable, non-antimicrobial
Model / Ref / Catalog
1525002
Primary DI / UDI-DI
M32815250020
FDA product code
FTM
GMDN term
Extra-gynaecological surgical mesh, collagen, bioabsorbable, non-antimicrobial
Device class
Class II
Regulation number
878.3300
GUDID distribution status
In Commercial Distribution
Size
Length — 15 Centimeter
Width — 25 Centimeter

Related devices

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

Similar devices

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

Other devices from Lifecell Corp

See all devices from Lifecell Corp →

Properties

  • Supplied sterile
  • Single use
  • Implantable
  • Prescription use
  • Lot / batch number
  • Expiration date
Other properties (9, all answered No)