Atlas FDA

Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account

Zest Anchors, LLC — Predicate Candidate Screening

12 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.

102 daysmedian FDA review time
239 days90th percentile
12clearances measured
K-numberDeviceApplicantDecidedReview daysRecalls (K-match)
K260555LOCATOR® Angled AbutmentZest Anchors, LLC2026-04-09500
K252944LOCATOR® Angled AbutmentZest Anchors, LLC2025-10-15300
K250721LOCATOR® Angled AbutmentZest Anchors, LLC2025-08-201630
K243272LOCATOR Angled AbutmentZest Anchors, LLC2025-01-14900
K233587LOCATOR Angled Abutment (Various)Zest Anchors, LLC2024-06-032080
K220252High Retention Attachment SystemZest Anchors, LLC2022-04-14730
K213391High Retention Attachment SystemZest Anchors, LLC2022-01-11880
K191619TurboTemp EZZest Anchors, LLC2019-09-11850
K151789LOCATOR F-Tx Attachment SystemZest Anchors, LLC2016-03-042470
K133327SATURNO(TM) OVERDENTURE IMPLANT SYSTEMZest Anchors, LLC2014-06-252390
K140570CHAIRSIDE ATTACHMENT PROCESSING MATERIALZest Anchors, LLC2014-06-161020
K120198LOCATOR OVERDENTURE IMPLANT SYSTEMZest Anchors, LLC2012-06-061350

Methodology

Recall counts reflect FDA recall records explicitly referencing each K-number; FDA links recalls to K-numbers inconsistently, so 0 means "none found in FDA records," not "never recalled." Data: FDA openFDA, refreshed weekly. Verify decisions of consequence against the primary source. Full candidate set and CSV export: atlasbyauro.com.

Prepared with Atlas

Predicate research, review-time statistics and recall monitoring for 510(k) teams — atlasbyauro.com/fda