Class Class II
LOCATOR® Angled Abutment (K250721)
Description
LOCATOR® Angled Abutment by Zest Anchors, LLC, an FDA 510(k) cleared dental device.
Regulatory Information
Device ClassClass Class II
510(k) NumberK250721
Clearance Date2025-08-20
Clearance TypeTraditional
Product CodeNHA
Regulation Number872.3630
FDA Database
View on FDA DatabaseCategories
Predicate lineage for K250721
A 510(k) clearance is granted by showing substantial equivalence to an earlier legally marketed device, called the predicate. This lineage is named in the 510(k) summary document and is not published by the FDA as a connected dataset. LOCATOR® Angled Abutment (K250721) cites 4 predicate devices and is itself cited by 0 later devices.
Predicate devices cited by this clearance
| K number | Device | Applicant | Year |
|---|---|---|---|
| K243272 | LOCATOR Angled Abutment | Zest Anchors, LLC | 2025 |
| K233587 | LOCATOR Angled Abutment (Various) | Zest Anchors, LLC | 2024 |
| K213391 | High Retention Attachment System | Zest Anchors, LLC | 2022 |
| K130572 | INTERACTIVE/ SWISHPLUS2 IMPLANT SYSTEM | Implant Direct Sybron Manufacturing... | 2013 |
Trace the full predicate network for K250721
A link appears here only where the predicate could be read from a published 510(k) summary. Where no summary exists or a reference cannot be resolved to a K number, no link is drawn, so a gap means unknown rather than none.