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

MAUDE Adverse Event Report: ZimVie US Corp LLC CERTAIN® TITANIUM LARGE HEXED SCREW; Dental Screw

  • 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
 

ZimVie US Corp LLC CERTAIN® TITANIUM LARGE HEXED SCREW; Dental Screw Back to Search Results
Catalog Number ILRGHT
Medical Device Problem Code Fracture (1260)
Health Effect - Clinical Code No Clinical Signs, Symptoms or Conditions (4582)
Date of Event 06/25/2026
Type of Reportable Event Malfunction
Search Alerts/Recalls

  New Search  |  Submit an Adverse Event Report

Brand Name
CERTAIN® TITANIUM LARGE HEXED SCREW
Common Device Name
Dental Screw
Manufacturer (Section D)
ZimVie US Corp LLC
4555 riverside drive
palm beach gardens FL 33410
Manufacturer (Section G)
ZimVie US Corp LLC
4555 riverside drive
palm beach gardens FL 33410
Manufacturer Contact
mark mashburn
4555 riverside drive
palm beach gardens, FL 33410
+1(561)971-3230
MDR Report Key50299922
Report Number0001038806-2026-04308
Device Sequence Number21513777
Product Code DZE
UDI-Device Identifier00844868006138
Combination Product (Y/N)N
Initial Reporter CountryGM
PMA/510(K) Number
K972444
Exemption Number5645646
Number of Events Summarized1
Summary Report (Y/N)N
Serviced by Third Party (Y/N)N
Reporter Type Manufacturer
Report Source Foreign,Health Professional
Initial Reporter Occupation Dentist
Type of Report Initial
Report Date (Section B) 08/18/2026
1 Device was Involved in the Event
1 Patient was Involved in the Event
Is this an Adverse Event Report? No
Is this a Product Problem Report? Yes
Operator of Device Lay User/Patient
Device Catalogue NumberILRGHT
Device Lot Number1299290
Was Device Available for Evaluation? Yes
Date Returned to Manufacturer07/28/2026
Is the Reporter a Health Professional? Yes
Initial Date Received by Manufacturer 07/28/2026
Initial Report FDA Received Date08/18/2026
Was Device Evaluated by Manufacturer? (Y/N) No
Date Device Manufactured04/28/2025
Is the Device Labeled for Single Use? (Y/N) No
Is This a Single-Use Device that was
Reprocessed and Reused on a Patient? (Y/N)
No
Usage of Device Unknown
Patient Sequence Number1
Patient Age65 YR
Patient SexMale
-
-