Flowable Restorative Material (KP-Flow LF, KP-Flow MF, KP-Flow HF)— 510(k) K261695

Name: FDA 510(k) clearance K261695
Creator: U.S. Food and Drug Administration
Published: 2026-08-31

Substantially Equivalent

Guilin Kevin Peter Technology Co., Ltd.

FDA 510(k) clearance K261695 for Flowable Restorative Material (KP-Flow LF, KP-Flow MF, KP-Flow HF), Substantially Equivalent on 2026-08-31. Applicant: Guilin Kevin Peter Technology Co., Ltd.. Device class: 2.

Clearance details

Applicant: Guilin Kevin Peter Technology Co., Ltd.
Product code: Code EBF
Device class: Class 2
Regulation: 21 CFR 872.3690
Advisory panel: Dental
Date received: 2026-05-22
Decision date: 2026-08-31
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Guilin, CN

Download summary PDF View on FDA.gov ↗

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