FDA Device Intelligence
Home › Medicon eG. Chirurgiemechaniker-Genossenschaft › Medicon

Medicon

Medicon eG. Chirurgiemechaniker-Genossenschaft · Model 76.50.00 · UDI-DI 04046826151645

HXY Prescription
7
510(k) clearances
44
Adverse events
1
Recalls
93
Facilities

Description

Stille bone drill cpl

Recalls

DateFirmReason
2015-05-27Musculoskeletal Transplant Foundation, Inc.Musculoskeletal Transplant Foundation is recalling a certain lot of Allofix Insertion Kits because they are labeled as having a 2.0mm diameter drill however it may contain a 2.4 mm

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.