ZenSeal Pro— 510(k) K252890

Substantially Equivalent

Kerr Corporation

FDA 510(k) clearance K252890 for ZenSeal Pro, Substantially Equivalent on 2026-01-07. Applicant: Kerr Corporation. Device class: 2.

Clearance details

Applicant: Kerr Corporation
Product code: Code KIF
Device class: Class 2
Regulation: 21 CFR 872.3820
Advisory panel: Dental
Date received: 2025-09-11
Decision date: 2026-01-07
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Pomona, 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.