MAUDE Adverse Event Report: THOMMEN MEDICAL AG ELEMENT IMPL., PF Ø 4.5, E Ø 4.2, L 11.0; DENTAL IMPLANT

Model Number 4.13.911

Device Problem Break (1069)

Patient Problem No Code Available (3191)

Event Date 05/06/2019

Event Type  Injury  

Event Description

Implant achieved osseointegration, primary stability was achieved, implant was completely covered with bone, implant fracture.

• Brand Name: ELEMENT IMPL., PF Ø 4.5, E Ø 4.2, L 11.0
• Type of Device: DENTAL IMPLANT
• Manufacturer (Section D): THOMMEN MEDICAL AG; neckarsulmstrasse 28; grenchen 2540 ; CH 2540
• Manufacturer (Section G): THOMMEN MEDICAL AG; neckarsulmstrasse 28; grenchen 2540 ; CH 2540
• Manufacturer Contact: astrid weber ; neckarsulmstrasse 28; grenchen 2540 ; CH 2540
• MDR Report Key: 9075128
• MDR Text Key: 158776862
• Report Number: 3003184527-2019-01199
• Device Sequence Number: 1
• Product Code: DZE
• UDI-Device Identifier: 07640156471489
• UDI-Public: 7640156471489
• Combination Product (y/n): N
• Reporter Country Code: IT
• PMA/PMN Number: K072649
• Number of Events Reported: 1
• Summary Report (Y/N): N
• Report Source: Manufacturer
• Source Type: health professional
• Reporter Occupation: Dentist
• Type of Report: Initial
• Report Date: 09/04/2019

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
• Device Operator: Health Professional
• Device Expiration Date: 08/12/2013
• Device Model Number: 4.13.911
• Device Lot Number: 5206
• Was Device Available for Evaluation?: Yes
• Is the Reporter a Health Professional?: Yes
• Was the Report Sent to FDA?: No
• Initial Date Manufacturer Received: 09/04/2019
• Initial Date FDA Received: 09/17/2019
• Was Device Evaluated by Manufacturer?: No
• Date Device Manufactured: 08/12/2008
• Is the Device Single Use?: Yes
• Is This a Reprocessed and Reused Single-Use Device?: No
• Type of Device Usage: Initial
• Patient Sequence Number: 1
• Patient Outcome(s): Other
• Patient Age: 74 YR