FDA Device Intelligence
Home › Avalign Technologies, Inc. › Millennium

Millennium

Avalign Technologies, Inc. · Model 72-452112 · UDI-DI 00190776394363

HCD
3
510(k) clearances
20
Adverse events (1 deaths)
0
Recalls
18
Facilities

Description

Cone Ventricular Needle, 3 1/2" (89mm) WL, 2 distal holes, 16g

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.