K-number	K253100
Device name	MultiPulse TFL
Applicant	Asclepion Laser Technologies GmbH
Product code	GEX
Device class	Class II
Decision date	Oct 23, 2025
Decision	Substantially Equivalent
Regulation	878.4810

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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MultiPulse TFL

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