Home › Davol Inc. › XENMATRIX
XENMATRIX
Davol Inc. · Model 1160606 · UDI-DI 00801741074332
1
510(k) clearances
3
Adverse events
1
Recalls
11
Facilities
Description
XenMatrix Surgical Graft, 6 cm x 6 cm (2.4" x 2.4"), Square
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. |
Query this across every FDA database — by API.
Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.
Get your free API keyRead the docsData 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.
