• Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

MAUDE Adverse Event Report: THOMMEN MEDICAL AG CONTACT IMPL., PF 3.5, E Ø 2.7, L 12.5; DENTAL IMPLANT

  • Print
  • Share
  • E-mail
-
Super Search Devices@FDA
510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
CFR Title 21 | Radiation-Emitting Products | X-Ray Assembler | Medsun Reports | CLIA | TPLC
 

THOMMEN MEDICAL AG CONTACT IMPL., PF 3.5, E Ø 2.7, L 12.5; DENTAL IMPLANT Back to Search Results
Model Number 4.13.230
Device Problem Break (1069)
Patient Problem Inadequate Osseointegration (2646)
Event Date 11/16/2022
Event Type  Injury  
Event Description
Implant fracture, loss of osseointegration, primary stability was achieved, implant was completely covered with bone, pain, increased sensitivity.
 
Search Alerts/Recalls

  New Search  |  Submit an Adverse Event Report

Brand Name
CONTACT IMPL., PF 3.5, E Ø 2.7, L 12.5
Type of Device
DENTAL IMPLANT
Manufacturer (Section D)
THOMMEN MEDICAL AG
neckarsulmstrasse 28
grenchen 2540
CH  2540
Manufacturer (Section G)
THOMMEN MEDICAL AG
neckarsulmstrasse 28
grenchen 2540
CH   2540
Manufacturer Contact
astrid weber
neckarsulmstrasse 28
grenchen 2540
CH   2540
MDR Report Key17556095
MDR Text Key321237549
Report Number3003184527-2023-01672
Device Sequence Number1
Product Code DZE
UDI-Device Identifier07640156471656
UDI-Public07640156471656
Combination Product (y/n)N
Reporter Country CodeIT
PMA/PMN Number
K072649
Number of Events Reported1
Summary Report (Y/N)N
Report Source Manufacturer
Source Type Health Professional
Reporter Occupation Dentist
Type of Report Initial
Report Date 04/25/2023
1 Device was Involved in the Event
1 Patient was Involved in the Event
Date FDA Received08/16/2023
Is this an Adverse Event Report? Yes
Is this a Product Problem Report? No
Device Operator Health Professional
Device Model Number4.13.230
Device Lot Number16658
Was Device Available for Evaluation? Yes
Is the Reporter a Health Professional? Yes
Was the Report Sent to FDA? No
Date Manufacturer Received04/25/2023
Was Device Evaluated by Manufacturer? No
Date Device Manufactured10/11/2017
Is the Device Single Use? Yes
Is This a Reprocessed and Reused Single-Use Device? No
Type of Device Usage Initial
Patient Sequence Number1
Patient Outcome(s) Other;
Patient Age75 YR
Patient SexFemale
Patient EthnicityNon Hispanic
Patient RaceWhite
-
-