Xenmatrix 1150816
by Davol Inc.
Xenmatrix 1150816 is a Class II device made by Davol Inc., listed in FDA GUDID since 8 Mar 2017 (UDI-DI 00801741128981), registry data as of 22 Oct 2026.
Listed
Valid until
Not applicable
FDA recalls
Not checked
Documents
None
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number00801741128981 | Date8 Mar 2017 | StatusListed |
Official records
- AccessGUDID record 00801741128981
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Xenmatrix
- Generic name
- Extra-gynaecological surgical mesh, collagen, bioabsorbable, antimicrobial
- Model / Ref / Catalog
- 1150816
- Primary DI / UDI-DI
- 00801741128981
- FDA product code
- PIJ, FTM, OXH
- 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 — 16 CentimeterLength — 8 Centimeter
Similar devices
Other devices filed under FDA product code FTM.
- XenMatrix AB Surgical Graft by C. R. Bard, Inc.
- FORTIVA PORCINE DERMIS, TUTOPLAST PORCINE DERMIS by Rti Surgical, Inc.
- BIOBLANKET by Kensey Nash Corp.
- VICRYL (POLYGLACTIN 910/MERSILENE COMPOISITE MESH by Ethicon Inc.
- PERI-GUARD, CV PERI-GUARD, OCU-GUARD, SUPPLE PERI-GUARD, PERI-STRIPS - SLEEVE, PERI-STRIPS-STRIPS, PERI-STRIPS DRY, VASC by Bio-Vascular, Inc.
- Biodesign Diaphragmatic Hernia Graft by COOK BIOTECH INCORPORATED
- TISSUEMEND SOFT TISSUE REPAIR MATRIX by TEI BIOSCIENCES INC.
- MECRON(R) ACETABULAR NETS TM by Serrano Intl.
- SYNTHES (USA) POROUS POLYETHYLENE IMPLANTS by Synthes (Usa)
- WMT COLLAGEN DERMAL MATRIX, 4 CM X 7 CM, MODEL 89XM-4X07, VMT COLLAGEN DERMAL MATRIX, 6 CM X 8 CM, MODEL 89XM-6X08 by AMERICAN MEDICAL SYSTEMS, INC.