Zest Anchors, Llc
2875 Loker Avenue East, Carlsbad, CA, US
Registered product codes
29 product codes
Recent MDR events
3,945 on file
- IMPLANT, ENDOSSEOUSJul 27, 2026Injury2023950-2026-00064
- IMPLANT, ENDOSSEOUSJul 27, 2026Injury2023950-2026-00068
- IMPLANT, ENDOSSEOUSJul 27, 2026Injury2023950-2026-00072
- IMPLANT, ENDOSSEOUSJul 27, 2026Injury2023950-2026-00067
- IMPLANT, ENDOSSEOUSJul 27, 2026Injury2023950-2026-00066
- IMPLANT, ENDOSSEOUSJul 27, 2026Injury2023950-2026-00073
- IMPLANT, ENDOSSEOUSJul 27, 2026Injury2023950-2026-00065
- IMPLANT, ENDOSSEOUSJul 27, 2026Injury2023950-2026-00069
- IMPLANT, ENDOSSEOUSJul 27, 2026Injury2023950-2026-00071
- IMPLANT, ENDOSSEOUSJul 27, 2026Injury2023950-2026-00070
Recalls
2 on file
- TerminatedFeb 6, 2014
Zest Anchors, LLC is voluntarily recalling specific lots of LOCATOR Implant Attachment Systems because it is currently provided with a label that indicates that the final torque applied to the abutment should be 30 N-cm. It was recently noted by Zest that in order to provide an optimal performance by increasing the factor of safety between the failure load of the abutment screw and the recommend
View FDA record ↗ - Open, ClassifiedUnknown
The abutment provided with the Implant System may be out of specification, which could lead to a small gap occurring between the implant and abutment on assembly in the patient.
View FDA record ↗
Compliance history
Matched by FEI 2023950.
FDA inspections
0 on file
No inspections on file for this FEI number.
Inspection citations
0 on file
No citations on file for this FEI number.
Compliance actions
0 on file
No warning letters or injunctions on file for this FEI number.
Import refusals
0 on file
No import refusals on file for this FEI number.