K-number	K251323
Device name	Device 104 Particulate
Applicant	Geistlich Pharma AG
Product code	KGN
Device class	Class U
Decision date	Jan 22, 2026
Decision	Substantially Equivalent
Regulation	—

AI Summary

The FDA summary PDF for this submission is not available in machine-readable form — common for older clearances. View on FDA's site →

Source

View the full FDA submission: accessdata.fda.gov

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Device 104 Particulate

Everything you need for a 510(k) submission. Nothing you don't.