TurboTemp EZ— 510(k) K191619

Substantially Equivalent

Zest Anchors, LLC

FDA 510(k) clearance K191619 for TurboTemp EZ, Substantially Equivalent on 2019-09-11. Applicant: Zest Anchors, LLC. Device class: 2.

Clearance details

Applicant: Zest Anchors, LLC
Product code: Code EBG
Device class: Class 2
Regulation: 21 CFR 872.3770
Advisory panel: Dental
Date received: 2019-06-18
Decision date: 2019-09-11
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Carlsbad, CA, US

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.