MAUDE Adverse Event Report: ACE SURGICAL SUPPLY CO. INFINITY INTERNAL HEX IMPLANT; DENTAL IMPLANT

Model Number	204108
Medical Device Problem Code	Patient Device Interaction Problem (4001)
Health Effect - Clinical Code	Failure of Implant (1924)
Type of Reportable Event	Serious Injury
Additional Manufacturer Narrative
The reported event has been determined to be a post-placement/preload failure.This implant loss suggests that the source of the problem was likely to stem from no osseointegration.Additionally, other factors that may have contributed to the implant failure includes bone condition, patient oral hygiene, overall health or behavior.Proper intended use of the implant is described in its instructions for use.
Event or Problem Description
Bone quality was type iii.Time of loss in relation to the implantation was before prosthetic restoration.Primary stability was not achieved.Osseointegration was not achieved.Augmentation procedure was not performed at time of surgery.Dr used wrong size.

• Brand Name: INFINITY INTERNAL HEX IMPLANT
• Common Device Name: DENTAL IMPLANT
• Manufacturer (Section D): ACE SURGICAL SUPPLY CO.; 1034 pearl street; brockton MA 02301
• MDR Report Key: 11904111
• Report Number: 1287163-2021-00862
• Device Sequence Number: 3754929
• Product Code: DZE
• UDI-Device Identifier: 00614950004683
• UDI-Public: 00614950004683
• Combination Product (Y/N): N
• Initial Reporter State: MA
• Initial Reporter Country: US
• PMA/510(K) Number: K102981
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Serviced by Third Party (Y/N): N
• Reporter Type: Manufacturer
• Report Source: health professional
• Initial Reporter Occupation: Dentist
• Type of Report: Initial

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: No Information
• Device Model Number: 204108
• Device Catalogue Number: 204108
• Device Lot Number: 20040003
• Was Device Available for Evaluation?: Device Returned to Manufacturer
• Date Returned to Manufacturer: 05/14/2021
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 05/14/2021
• Initial Report FDA Received Date: 05/28/2021
• 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: 81 YR