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

Anmuth Medical International

Anmuth Medical International, LLC · Model 38-826-00 · UDI-DI 08403207008909

FFO
5
510(k) clearances
86
Adverse events
3
Recalls
152
Facilities

Description

CHARNLEY Retractor Complete with Weight

Recalls

DateFirmReason
2024-12-03Sklar InstrumentsReports of various packaging issues that may result in a breach of the sterile barrier.
2015-11-25Abeon Medical CorporationThe firm was notified by some of their customers that some of the sealed pouches contain tears compromising the sterility of the product.
2015-11-25Abeon Medical CorporationThe firm was notified by some of their customers that some of the sealed pouches contain tears compromising the sterility of the product.

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.