510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K140570Substantially Equivalent

Chairside Attachment Processing Material

Zest Anchors LLC, San Diego CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K140570 is the FDA 510(k) clearance record for CHAIRSIDE ATTACHMENT PROCESSING MATERIAL, a class II device, cleared for Zest Anchors, LLC on under FDA product code EBI (Resin, Denture, Relining, Repairing, Rebasing). FDA records list 26 510(k) clearances for Zest Anchors, LLC, from to . As of , FDA records show no recalls naming K140570.

Clearance record

Decision date
Received
(102 days to decision)
Product code
EBI Resin, Denture, Relining, Repairing, Rebasing
Regulation
21 CFR 872.3760
Device class
Class II
Review panel
Dental
Applicant
Zest Anchors, LLC 12264 El Camino Real, San Diego CA
510(k) summary
Summary PDF
Third party review
No

Clearances, product code EBI

Trailing 12 months
10 clearances under product code EBI in the twelve months to October 2026, November 2025 the highest month at 3.
Show the numbers
Monthly 510(k) clearances under FDA product code EBI, trailing twelve months
MonthClearances
November 20253
December 20250
January 20260
February 20260
March 20260
April 20260
May 20261
June 20261
July 20263
August 20262
September 20260
October 20260