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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: ALTATEC GMBH CAMLOG CYLINDER-LINE IMPLANT

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ALTATEC GMBH CAMLOG CYLINDER-LINE IMPLANT Back to Search Results
Model Number J1011.5016
Medical Device Problem Code Loss of Osseointegration (2408)
Health Effect - Clinical Code No Clinical Signs, Symptoms or Conditions (4582)
Date of Event 02/19/2026
Type of Reportable Event Serious Injury
Event or Problem Description
Loss of osseointegration (dental implant).
 
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Brand Name
CAMLOG CYLINDER-LINE IMPLANT
Common Device Name
CAMLOG CYLINDER-LINE IMPLANT
Manufacturer (Section D)
ALTATEC GMBH
maybachstrasse.5
wimsheim,
GM 
Manufacturer (Section G)
ALTATEC GMBH
maybachstrasse.5
wimsheim, 71299
GM   71299
Manufacturer Contact
monika hentschel
maybachstrasse 5
wimsheim, 71299
GM   71299
MDR Report Key24738499
Report Number9613866-2026-50435
Device Sequence Number9790724
Product Code DZE
Combination Product (Y/N)N
Initial Reporter CountryGM
Number of Events Summarized1
Summary Report (Y/N)N
Device Implanted Year2006
Device Explanted Year2026
Serviced by Third Party (Y/N)Unknown
Reporter Type Manufacturer
Report Source Health Professional
Initial Reporter Occupation Dentist
Type of Report Initial
Report Date (Section B) 03/30/2026
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 NumberJ1011.5016
Device Lot NumberFF04000830
Was Device Available for Evaluation? Yes
Is the Reporter a Health Professional? Yes
Type of Report(Section G)Thirty-Day
Initial Date Received by Manufacturer 03/17/2026
Initial Report FDA Received Date03/31/2026
Was Device Evaluated by Manufacturer? (Y/N) No
Is the Device Labeled for Single Use? (Y/N) Yes
Is This a Single-Use Device that was
Reprocessed and Reused on a Patient? (Y/N)
No
Usage of Device Initial
Patient Sequence Number1
Outcome Attributed to Adverse Event Required Intervention;
Patient Age54 YR
Patient SexFemale
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