Xtreem Pulse, LLC

Xtreem Pulse, LLC holds 5 FDA 510(k) medical device clearances, first cleared 2018, most recent 2026.

Top product codes for Xtreem Pulse, LLC

NFO — Neurology4 devices
DRN — Cardiovascular1 device

Recent clearances by Xtreem Pulse, LLC

K262861 — PureLift Pro MaxCode NFO·2026-09-11
K243587 — PureLift GLOWCode NFO·2025-03-06
K221443 — PureLift Pro PlusCode NFO·2022-10-21
K190269 — PureLiftCode NFO·2019-08-28
K173483 — Pure Flow External Counter-Pulsation DeviceCode DRN·2018-05-30

Data sourced from openFDA. This site is unofficial and independent of the FDA.