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

Millennium

Avalign Technologies, Inc. · Model 85-78093537 · UDI-DI 00190776365158

EMJ Prescription
6
510(k) clearances
644
Adverse events
0
Recalls
242
Facilities

Description

Explorer, #23,

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.