FDA Device Intelligence
Home › MEDTRONIC XOMED, INC. › Bio-Flek

Bio-Flek

MEDTRONIC XOMED, INC. · Model 1358225 · UDI-DI 00763000299101

EPW Prescription
2
510(k) clearances
2
Adverse events
0
Recalls
10
Facilities

Description

HEAD SUPPORT 1358225 BIOFLEK SURGICAL

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.