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

Millennium

Avalign Technologies, Inc. · Model 1-30320 · UDI-DI 00190776406677

HDL
2
510(k) clearances
19
Adverse events
1
Recalls
120
Facilities

Description

Eastman Vaginal Retractor, blade 1.5" (3.8cm) x 3" (7.6cm), 7" OL

Recalls

DateFirmReason
2024-12-03Sklar InstrumentsReports of various packaging issues that may result in a breach of the sterile barrier.

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.