Recall Z-2204-2013— Camlog Usa

Name: FDA recall Z-2204-2013
Creator: U.S. Food and Drug Administration
Published: 2013-08-28

Class II · Terminated

Class II FDA medical device recall by Camlog Usa, initiated 2013-08-28, terminated 2014-01-29. FDA's recall record names no specific 510(k) clearance for this event. Product: C2244.3820;, CONELOG Titanium Base CC ¿3.8GH2.0 inkl HS Product Usage: Endosseous dental implant abutment CONELOG Abutments are intended to be used to fabricate prosthetic restorations in conjunction with CONELOG implants to support prostheses in the maxillary and/or mandibular arch.. Reason: Product not cleared for sale/use in the United States..

Recalling firm: Camlog Usa
Classification: Class II
Status: Terminated
Initiated: 2013-08-28
Terminated: 2014-01-29
Firm location: Indianapolis, IN, United States

Product description

C2244.3820;, CONELOG Titanium Base CC ¿3.8GH2.0 inkl HS Product Usage: Endosseous dental implant abutment CONELOG Abutments are intended to be used to fabricate prosthetic restorations in conjunction with CONELOG implants to support prostheses in the maxillary and/or mandibular arch.

Reason for recall

Product not cleared for sale/use in the United States.

Data sourced from openFDA. This site is unofficial and independent of the FDA.