RegWardenFDA facility compliance records
Facility

ZEST ANCHORS, LLC

2 recall(s) on record — most severe on record: Class II.

Activity by year

FDA actions on record by year2014: 1 recalls; 2019: 1 recalls1’14’15’16’17’181’19’20’21’22’23’24’25’26
  • Recalls (2)

Devices registered here (1)

Recalls & enforcement

  • Class IIOngoing2019-11-22
    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.
  • Class IITerminated2014-01-16
    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 …

Related

Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this facility record at FDA → (opens in a new tab)

Cite this record

RegWarden. “ZEST ANCHORS, LLC (FEI 2023950) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/2023950-zest-anchors-llc/

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