FDA Device Intelligence
HomeAvalign Technologies, Inc. › Avalign

Avalign

Avalign Technologies, Inc. · Model VM81-2072 · UDI-DI 00190776136000

HAE Prescription
10
510(k) clearances
482
Adverse events (1 deaths)
2
Recalls
64
Facilities

Description

Micro Kerrison, Angled up 40 degrees, 15mm Jaw Opening, TW 5mm (1/4"), SL 255mm (10"), OL 315mm (12 1/2")

Recalls

DateFirmReason
2023-10-30Folsom Metal Products, Inc.Units were not intended for commercial distribution and inadvertently distributed.
2023-10-30Folsom Metal Products, Inc.Units were not intended for commercial distribution and inadvertently distributed.

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.