MAUDE Adverse Event Report: ALTATEC ALTATEC; DENTAL IMPLANT

Model Number	C1086.4311
Medical Device Problem Code	Use of Device Problem (1670)
Health Effect - Clinical Code	Insufficient Information (4580)
Date of Event	03/06/2026
Type of Reportable Event	Serious Injury
Additional Manufacturer Narrative
The delay in submission was due to a system issue involving the generation of duplicate report numbers.The vendor, honeywell sparta, was notified after several emdr records failed to submit.At the vendor¿s request, submission of similar records was temporarily halted while the root cause was investigated, and a corrective solution was developed.Prior to identification of the system issue, the affected records were on track for timely submission.Due to the time required for vendor investigation, root cause analysis, and implementation of a corrective action, the records subsequently became past due.The corrective fix has now been deployed within the system.Newly created records are functioning as expected, and the vendor is actively monitoring system performance as a precaution.
Event or Problem Description
Implant removed due to surgical consideration within 36 hours.

• Brand Name: ALTATEC
• Common Device Name: DENTAL IMPLANT
• Manufacturer (Section D): ALTATEC; maybachstrasse 5; wimsheim 71299 ; GM 71299
• MDR Report Key: 25152420
• Report Number: 1060818-2026-60155
• Device Sequence Number: 9213308
• Product Code: DZE
• UDI-Device Identifier: E219C108643111
• UDI-Public: E219C108643111
• Combination Product (Y/N): N
• Initial Reporter State: CO
• Initial Reporter Country: US
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Device Implanted Year: 2026
• Device Explanted Year: 2026
• Serviced by Third Party (Y/N): N
• Reporter Type: Importer
• Initial Reporter Occupation: Dentist
• Type of Report: Initial
• Report Date (Section B): 04/05/2026

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: Health Professional
• Device Model Number: C1086.4311
• Device Catalogue Number: C1086.4311
• Device Lot Number: 0010409870
• Is the Reporter a Health Professional?: Yes
• Distributor Facility Aware Date: 03/06/2026
• Initial Date Received by Manufacturer: Not provided
• Initial Report FDA Received Date: 05/12/2026
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Usage of Device: A
• Patient Sequence Number: 1
• Outcome Attributed to Adverse Event: Required Intervention
• Patient Sex: Unknown