Atlas FDA

Camlog Usa

4 FDA 510(k) clearances · Recalling firm

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RecordFirmDate
C2244.3808, CONELOG Titanium Base CC 3.8GH0.8 inkl HS Product Usage: Endosseous dental imp recall (Z-2203-2013)Camlog Usa2013-09-16
C2244.3820;, CONELOG Titanium Base CC 3.8GH2.0 inkl HS Product Usage: Endosseous dental im recall (Z-2204-2013)Camlog Usa2013-09-16
C2244.4308 CONELOG Titanium Base CC 4.3GH2 0.8 inkl HS Product Usage: Endosseous dental im recall (Z-2205-2013)Camlog Usa2013-09-16
C2244.5008 CONELOG Titanbasis CAD/CAM Conelog Titanium Base CAD/CAM Rx only 5.0GH 0.8 inkl recall (Z-2206-2013)Camlog Usa2013-09-16

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Every clearance here is in the API, with alerts when new ones post.