FDA Device Intelligence
HomeDavol Inc. › XENMATRIX

XENMATRIX

Davol Inc. · Model 1152025 · UDI-DI 00801741074288

PIJFTMOXH Prescription
3
510(k) clearances
83
Adverse events (4 deaths)
0
Recalls
5
Facilities

Description

XenMatrix AB Surgical Graft, 20 cm x 25 cm

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 docs
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.