MAUDE Adverse Event Report: HIOSSEN INC. ET III SA FIXTURE; DENTAL IMPLANT

Model Number	CET3R4013S
Health Effect - Clinical Code	Bone Fracture(s) (1870)
Date of Event	05/30/2017
Type of Reportable Event	Serious Injury
Additional Manufacturer Narrative
It is reported to hiossen that a fracture had been occurred to patient in her at (b)(6)'s by dental office located in (b)(6).Hiossen had investigated using the record pertaining to this batch number : device history record , manufacturing batch record, all inspection records, raw material record, all return record related unsuccessful implantation in same batch.The implant has significant bone lose in 5 months period that is shown on the x-ray this crown is above the natural teeth and may be taking all of the chewing force that may have caused the fracture.All of records showed that there were no fracture related problem.The implant were manufactured according to the standard and all acceptance criteria have been met the required specifications.Scientific, advisory board review: hiossen's scientific advisory board reviewed the available material ( i.E.Radiographs ) and theorized the potential reasons behind the implant fracture.Possible causes of fixture fracturing based on the material provided (radiographs ).It is assumed that there were several possibilities that caused the fracture.Insufficient crestal hard tissue to support the upper portion of the implant from mystification & sheering forces.Overloading or bruxism could have attributed to the fracturing of the implant.
Event or Problem Description
It was reported that the placed implant had been fractured in the patient's mouth after 4 years of implantation.

• Brand Name: ET III SA FIXTURE
• Common Device Name: DENTAL IMPLANT
• Manufacturer (Section D): HIOSSEN INC.; 85 ben fairless dr.; fairless hills PA 19030
• MDR Report Key: 7527575
• Report Number: 3007135442-2017-00002
• Device Sequence Number: 11175772
• Product Code: DZE
• UDI-Device Identifier: 00814913021058
• UDI-Public: 00814913021058
• Combination Product (Y/N): N
• Initial Reporter State: MI
• Initial Reporter Country: US
• PMA/510(K) Number: K140934
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Device Implanted Year: 2013
• Device Explanted Year: 2017
• Reporter Type: Manufacturer
• Report Source: health professional
• Initial Reporter Occupation: Dentist
• Remedial Action: Inspection
• Type of Report: Initial
• Report Date (Section B): 04/17/2017

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Is this an Adverse Event Report?: Yes
• Is this a Product Problem Report?: No
• Operator of Device: Dentist
• Device Expiration Date: 08/19/2017
• Device Model Number: CET3R4013S
• Device Lot Number: H1E12F117
• Was Device Available for Evaluation?: Device Returned to Manufacturer
• Date Returned to Manufacturer: 07/05/2017
• Was the Report Sent to FDA?: No
• Type of Report(Section G): Initial
• Initial Date Received by Manufacturer: 07/05/2017
• Initial Report FDA Received Date: 05/18/2018
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Patient Sequence Number: 1
• Outcome Attributed to Adverse Event: Required Intervention
• Patient Age: 63 YR