MAUDE Adverse Event Report: ALTATEC ALTATEC; DENTAL IMPLANT

Model Number	K1056.3811
Medical Device Problem Code	Failure to Osseointegrate (1863)
Health Effect - Clinical Code	Insufficient Information (4580)
Date of Event	01/08/2026
Type of Reportable Event	Serious Injury
Additional Manufacturer Narrative
System experienced an internal error in submission.The system provider salesforce trackwise was notified under support case (b)(4) to address.It was determined a new email address was needed that did not require a change in password.Trackwise support indicated anytime a password occurs with the associated email address an internal error will be received.To fix the issue, a new biohorizons forwarding email address that did not require a change in password at any time.The effort was performed to update the email address.It is believed this records were impacted why the change to email was being impacted.
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: 24960517
• Report Number: 1060818-2026-60042
• Device Sequence Number: 13422761
• Product Code: DZE
• UDI-Device Identifier: E219K105638111
• UDI-Public: E219K105638111
• Combination Product (Y/N): N
• Initial Reporter State: LA
• Initial Reporter Country: US
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Device Implanted Year: 2025
• 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): 02/07/2026

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: K1056.3811
• Device Catalogue Number: K1056.3811
• Device Lot Number: 0020280429
• Was Device Available for Evaluation?: Yes
• Is the Reporter a Health Professional?: Yes
• Distributor Facility Aware Date: 01/08/2026
• Initial Date Received by Manufacturer: Not provided
• Initial Report FDA Received Date: 04/22/2026
• 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