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Mesh, Surgical, Collagen, Diaphragmatic Hernia

FDA product code OWV · Class 2 · General, Plastic Surgery

61

Registered devices

3

Adverse events

1

Recalls

1

510(k) clearances

Devices with this code

XENMATRIX — Davol Inc.Gentrix® — ACELL, INC.XENMATRIX — Davol Inc.VERITAS COLLAGEN MATRIX — SYNOVIS LIFE TECHNOLOGIES, INC.XENMATRIX — Davol Inc.VERITAS COLLAGEN MATRIX — SYNOVIS LIFE TECHNOLOGIES, INC.XENMATRIX — Davol Inc.XENMATRIX — Davol Inc.XENMATRIX — Davol Inc.XENMATRIX — Davol Inc.VERITAS COLLAGEN MATRIX — SYNOVIS LIFE TECHNOLOGIES, INC.Supple Peri-Guard — SYNOVIS LIFE TECHNOLOGIES, INC.Supple Peri-Guard — SYNOVIS LIFE TECHNOLOGIES, INC.XENMATRIX — Davol Inc.Gentrix® — ACELL, INC.Gentrix® — ACELL, INC.Supple Peri-Guard — SYNOVIS LIFE TECHNOLOGIES, INC.Peri-Guard — SYNOVIS LIFE TECHNOLOGIES, INC.Peri-Guard — SYNOVIS LIFE TECHNOLOGIES, INC.Peri-Guard — SYNOVIS LIFE TECHNOLOGIES, INC.Supple Peri-Guard — SYNOVIS LIFE TECHNOLOGIES, INC.XENMATRIX — Davol Inc.XENMATRIX — Davol Inc.Gentrix® — ACELL, INC.

Recent recalls

Date	Firm	Reason
2024-11-22	Cook Biotech, Inc.	Incorrect version of IFU was used rather than updated version; and incorrect expiration date was used on two of the products.

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Sourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.