Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Zest Anchors, Inc. · Predicate Candidate Screening
14 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.
102 daysmedian FDA review time
511 days90th percentile
14clearances measured
| K-number | Device | Applicant | Decided | Review days | Recalls (K-match) |
|---|---|---|---|---|---|
| K150295 | LOCATOR RTx | Zest Anchors, Inc. | 2015-07-24 | 168 | 0 |
| K083324 | LOCATOR IMPLANT ANCHOR ATTACHMENT SYSTEM | Zest Anchors, Inc. | 2009-02-25 | 105 | 0 |
| K072878 | MODIFICATION TO: LOCATOR IMPLANT ANCHOR | Zest Anchors, Inc. | 2007-12-03 | 55 | 1 |
| K042466 | X-2 IMPLANT ABUTMENT; BAR MALE; DISTAL EXTENSION MALE | Zest Anchors, Inc. | 2004-11-24 | 72 | 0 |
| K033699 | LOCATOR BAR FEMALE, LOCATOR LASER BAR FEMALE, LOCATOR BAR CA | Zest Anchors, Inc. | 2004-04-22 | 149 | 0 |
| K994257 | LOCATOR IMPLANT ANCHOR | Zest Anchors, Inc. | 2000-03-17 | 92 | 2 |
| K925849 | ZEST IMPLANT ANCHOR | Zest Anchors, Inc. | 1994-11-18 | 730 | 0 |
| K934668 | ZEST IMPLANT ANCHOR ADVANCED GENERATION (DENTAL) | Zest Anchors, Inc. | 1994-06-22 | 266 | 0 |
| K925700 | ZEST ANCHOR ADVANCED GENERATION | Zest Anchors, Inc. | 1994-04-07 | 511 | 0 |
| K882063 | MAGNE-DENT MAGNET/ZEST RETROFIT KEEPER | Zest Anchors, Inc. | 1988-06-13 | 28 | 0 |
| K861561 | ZEST MARK II (STANDARD & MINI) | Zest Anchors, Inc. | 1986-05-21 | 26 | 0 |
| K840244 | BIOCERAM ZEST PLANT | Zest Anchors, Inc. | 1984-05-01 | 102 | 0 |
| K801525 | ZEST ENDODONTIC STABILIZER | Zest Anchors, Inc. | 1980-07-21 | 20 | 0 |
| K801524 | ZEST PLANT | Zest Anchors, Inc. | 1980-07-21 | 20 | 0 |
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