FDA 510(k) Applications for Medical Device Product Code: PLH ()

FDA 510(k) Applications for Medical Device Product Code "PLH"

FDA 510(k) Number	Applicant	Device Name	Decision Date
K143120	BIOLUX RESEARCH LTD.	OrthoPulse	07/24/2015
K230905	Biolux Technology GmbH	OrthoPulse 2.0E (OPi2E-100)	06/09/2023

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