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OviTex® Low Profile

AROA BIOSURGERY LIMITED · Model F10264-0909L · UDI-DI 09421908222072

FTMFTL Prescription
1
510(k) clearances
11,594
Adverse events (47 deaths)
76
Recalls
89
Facilities

Description

The OviTex® Reinforced Tissue Matrix Device is a sterile reinforced matrix device comprised of non-dermal sourced layers of extracellular matrix (ECM) (ovine (sheep) derived ECM), paired with a minimal suture footprint. OviTex Reinforced Tissue Matrix Device provides an alternative device solution to permanent synthetic, resorbable/bioabsorbable synthetic, and biologic meshes. The device remodels and helps regenerate tissue while reinforcing the repair and providing structural support. Reinforced tissue matrices enhance performance while maintaining compatibility with the body. The OviTex Reinforced Tissue Matrix Device is used for hernia repair and abdominal wall reconstruction.

Recalls

DateFirmReason
2024-08-07Cook Biotech, Inc.Products expire prior to the expiration date printed on the product labeling
2024-08-07Cook Biotech, Inc.Products expire prior to the expiration date printed on the product labeling
2024-08-07Cook Biotech, Inc.Products expire prior to the expiration date printed on the product labeling
2024-08-07Cook Biotech, Inc.Products expire prior to the expiration date printed on the product labeling
2024-08-07Cook Biotech, Inc.Products expire prior to the expiration date printed on the product labeling
2024-08-07Cook Biotech, Inc.Products expire prior to the expiration date printed on the product labeling
2024-08-07Cook Biotech, Inc.Products expire prior to the expiration date printed on the product labeling
2024-08-07Cook Biotech, Inc.Products expire prior to the expiration date printed on the product labeling
2024-08-07Cook Biotech, Inc.Products expire prior to the expiration date printed on the product labeling
2024-08-07Cook Biotech, Inc.Products expire prior to the expiration date printed on the product labeling

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Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.