Xtreem Pulse, LLC FDA Approvals

0 new drug approvals and 3 device clearances on file. This applicant is not matched to a listed company.

Newest first

A new drug approval is an original application; a 510(k) is a device shown equivalent to one already sold.

Product	What it is	Route	Decided
PureLift Pro Max510(k)Sep 11, 2026Neurology	Neurology	510(k)Substantially Equivalent (Special)	Sep 11, 2026
PureLift GLOW510(k)Mar 6, 2025Neurology	Neurology	510(k)Substantially Equivalent (Traditional)	Mar 6, 2025
PureLift Pro Plus510(k)Oct 21, 2022Neurology	Neurology	510(k)Substantially Equivalent (Special)	Oct 21, 2022