MAUDE Adverse Event Report: ALTATEC ALTATEC; DENTAL IMPLANT

Model Number	C1086.3816
Medical Device Problem Code	Failure to Osseointegrate (1863)
Health Effect - Clinical Code	Insufficient Information (4580)
Date of Event	02/27/2026
Type of Reportable Event	Serious Injury
Additional Manufacturer Narrative
This record was discovered during the monitoring of the system.Records were unable to be transmitted due to a system issue with vendor.Vendor system failed to connect to the fda gateway timely and advised not to transmit until fixed.The issue was fixed and addressed.However, the assigned processor failed to transmit via the gateway when instructed.
Event or Problem Description
Implant failed to osseointegrate.

• Brand Name: ALTATEC
• Common Device Name: DENTAL IMPLANT
• Manufacturer (Section D): ALTATEC; maybachstrasse 5; wimsheim 71299 ; GM 71299
• MDR Report Key: 25209784
• Report Number: 1060818-2026-60217
• Device Sequence Number: 10565623
• Product Code: DZE
• UDI-Device Identifier: E219C108638161
• UDI-Public: E219C108638161
• Combination Product (Y/N): N
• Initial Reporter State: FL
• 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): 03/29/2026

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 Expiration Date: 08/17/2026
• Device Model Number: C1086.3816
• Device Catalogue Number: C1086.3816
• Device Lot Number: 0010113712
• Is the Reporter a Health Professional?: Yes
• Distributor Facility Aware Date: 02/27/2026
• Initial Date Received by Manufacturer: Not provided
• Initial Report FDA Received Date: 05/18/2026
• 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