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Recall Observatory FDA recall evidence

Device product

C2244.3808, CONELOG Titanium Base CC ¿3.8GH0.8 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.

Z-2203-2013

August 28, 2013

Class II

Product summary

Firm
Camlog Usa
Event
Event 66143
Status
Terminated
Classification
Class II
Quantity
2 in USA
Official record key
device-enforcement:Z-2203-2013

Official wording

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

Code information: 43746

Distribution pattern: USA Distribution in the states of NH, MD, CO, and IL.

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

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