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

Anmuth Medical International

Anmuth Medical International, LLC · Model 38-100-01 · UDI-DI 08403207006042

KBB
0
510(k) clearances
6
Adverse events
0
Recalls
82
Facilities

Description

Micro-FRIEDMAN Rongeur Str Delicate 14.5cm/5.5"

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.