Zest Anchors, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Zest Anchors, LLC - FDA 510(k) Cleared Devices
Recent clearances: LOCATOR® Angled Abutment, LOCATOR® Angled Abutment, LOCATOR® Angled Abutment
12
Total
12
Cleared
0
Denied
Zest Anchors, LLC has 12 FDA 510(k) cleared dental devices. Based in Escondido, US.
Latest FDA clearance: Apr 2026. Active since 2012.
Browse the complete list of FDA 510(k) cleared dental devices from this manufacturer. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by PaxMed International, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Zest Anchors, LLC
12 devices
Cleared
Apr 09, 2026
LOCATOR® Angled Abutment
Dental
50d
Cleared
Oct 15, 2025
LOCATOR® Angled Abutment
Dental
30d
Cleared
Aug 20, 2025
LOCATOR® Angled Abutment
Dental
163d
Cleared
Jan 14, 2025
LOCATOR Angled Abutment
Dental
90d
Cleared
Jun 03, 2024
LOCATOR Angled Abutment (Various)
Dental
208d
Cleared
Apr 14, 2022
High Retention Attachment System
Dental
73d
Cleared
Jan 11, 2022
High Retention Attachment System
Dental
88d
Cleared
Sep 11, 2019
TurboTemp EZ
Dental
85d
Cleared
Mar 04, 2016
LOCATOR F-Tx Attachment System
Dental
247d
Cleared
Jun 25, 2014
SATURNO(TM) OVERDENTURE IMPLANT SYSTEM
Dental
239d
Cleared
Jun 16, 2014
CHAIRSIDE ATTACHMENT PROCESSING MATERIAL
Dental
102d
Cleared
Jun 06, 2012
LOCATOR OVERDENTURE IMPLANT SYSTEM
Dental
135d