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SUPERLINE Adverse Event — Injury (MDR 3005503242-2020-00063)

SUPERLINE Adverse Event — Injury (MDR 3005503242-2020-00063) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: SUPERLINE; Generic name: DENTAL IMPLANT; Manufacturer: DENTIUMUSA.

DeviceSUPERLINE
Generic nameDENTAL IMPLANT
ManufacturerDENTIUMUSA
Report number3005503242-2020-00063
Event typeInjury
Product problemN
Date received2020-04-28
Report sourceHEALTH PROFESSIONAL
NarrativeTHE DENTAL IMPLANT FX4508SWC WAS REMOVED ON (B)(6) 2020 DUE TO OSSEOINTEGRATION FAILURE AROUND 3 MONTHS AND 6 DAYS AFTER IMPLANTATION. THE PATIENT HAS HISTORY OF HYPERTENSION. THE DOCTOR NOTED PERIODONTAL DISEASE DURING EXPLANTATION. THE PATIENT HAS RECOVERED WITHOUT COMPLICATIONS.
SourceopenFDA MAUDE (device adverse events)

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