FDA Device Intelligence
Home › Anmuth Medical International, LLC › Anmuth Medical International

Anmuth Medical International

Anmuth Medical International, LLC · Model 38-831-16 · UDI-DI 08403207008916

HTE
0
510(k) clearances
137
Adverse events (1 deaths)
3
Recalls
175
Facilities

Description

TAYLOR Spinal Lever 75x30mm 16.5cm/6.5"

Recalls

DateFirmReason
2013-09-24SpineFrontier, Inc.Handles and heads may not be compatible.
2013-09-24SpineFrontier, Inc.Handles and heads may not be compatible.
2013-09-24SpineFrontier, Inc.Handles and heads may not be compatible.

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.