Geistlich Bio-Flow®— 510(k) K242510

Substantially Equivalent

Geistlich Pharma AG

FDA 510(k) clearance K242510 for Geistlich Bio-Flow®, Substantially Equivalent on 2025-03-07. Applicant: Geistlich Pharma AG. Device class: 2.

Clearance details

Applicant: Geistlich Pharma AG
Product code: Code NPM
Device class: Class 2
Regulation: 21 CFR 872.3930
Advisory panel: Dental
Date received: 2024-08-23
Decision date: 2025-03-07
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Wolhusen, CH

Download summary PDF View on FDA.gov ↗

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More clearances from Geistlich Pharma AG

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