FDA Device Intelligence
HomeMedicon eG. Chirurgiemechaniker-Genossenschaft › Medicon

Medicon

Medicon eG. Chirurgiemechaniker-Genossenschaft · Model 68.72.62 · UDI-DI 04046826120733

JEY Prescription
10
510(k) clearances
10,393
Adverse events (21 deaths)
111
Recalls
105
Facilities

Description

Ti Mini Multi Grid plate square 1x2 segm 1.0mm p/2

Recalls

DateFirmReason
2023-06-19Materialise N.V.Wrong versions of guides 3A and 3B (Patient Specific) were shipped prior to the re-design request
2020-11-25Biomet, Inc.Specific lots of multiple sterile medical devices may have a breach in the sterile seal. A breach in the packaging seal could lead to loss of sterility of the device.
2020-06-18Synthes, Inc.One lot of MatrixNEURO 5mm screws was packaged in a body clip etched "4", which indicated a 4mm screw. The outer package labeling correctly identifies a 5mm screw, but the body clo
2020-06-16Synthes Produktions GmbHOne lot of MatrixMIDFACE Emergency Screw 1.8mm, self-tapp, L 12mm, in Clip was packaged with a body clip etched with a 3 (representing 3mm) when it should have been packaged with
2020-02-03Materialise N.V.Custom surgical kits contain a plate different than indicated by the package labeling.
2020-02-03Materialise N.V.Custom surgical kits contain a plate different than indicated by the package labeling.
2018-04-05Zimmer Biomet, Inc.The recalling firm has confirmed that the Outer Plate component exhibits an excessive chamfer on the threading after deburring operations. This excessive chamfer results in non-con
2016-05-02Synthes (USA) Products LLCLabeling errors. The outer packge label expiration date may exceed the expiration date of the subcomponents.
2016-05-02Synthes (USA) Products LLCLabeling errors. The outer packge label expiration date may exceed the expiration date of the subcomponents.
2016-05-02Synthes (USA) Products LLCLabeling errors. The outer packge label expiration date may exceed the expiration date of the subcomponents.

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.