K-number	K252430
Device name	Freeprint® denture flex
Applicant	Detax GmbH
Product code	EBI
Device class	Class II
Decision date	Oct 30, 2025
Decision	Substantially Equivalent
Regulation	872.3760

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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Freeprint® denture flex

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