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

MAUDE Adverse Event Report: BIOHORIZONS INC. BIOHORIZONS INC.; 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
 

BIOHORIZONS INC. BIOHORIZONS INC.; DENTAL IMPLANT Back to Search Results
Model Number 400-200
Medical Device Problem Code No Apparent Adverse Event (3189)
Health Effect - Clinical Code Insufficient Information (4580)
Date of Event 06/04/2024
Type of Reportable Event Serious Injury
Event or Problem Description
Autotac handle doesn't cock correctly, and the button keeps popping back up.
 
Search Alerts/Recalls

  New Search  |  Submit an Adverse Event Report

Brand Name
BIOHORIZONS INC.
Common Device Name
DENTAL IMPLANT
Manufacturer (Section D)
BIOHORIZONS INC.
2300 riverchase center
birmingham AL 35244
Manufacturer (Section G)
BIOHORIZONS INC.
2300 riverchase center
birmingham AL 35244
Manufacturer Contact
anissa smith
2300 riverchase center
birmingham, AL 35244
MDR Report Key20267167
Report Number1060818-2024-12826
Device Sequence Number20636110
Product Code DZE
UDI-Device Identifier00847236010218
UDI-Public00847236010218
Combination Product (Y/N)N
Initial Reporter StateOH
Initial Reporter CountryUS
PMA/510(K) Number
K022790
Number of Events Summarized1
Summary Report (Y/N)N
Serviced by Third Party (Y/N)N
Reporter Type Manufacturer
Report Source Company Representative
Initial Reporter Occupation Dentist
Type of Report Initial
Report Date (Section B) 07/04/2024
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 Number400-200
Device Catalogue Number400-200
Device Lot Number2302790D
Is the Reporter a Health Professional? Yes
Type of Report(Section G)Thirty-Day
Initial Date Received by Manufacturer 06/04/2024
Initial Report FDA Received Date09/20/2024
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 SexUnknown
-
-