Xtreem Pulse, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Xtreem Pulse, LLC - FDA 510(k) Cleared Devices
Recent clearances: PureLift GLOW, PureLift Pro Plus, PureLift
4
Total
4
Cleared
0
Denied
Xtreem Pulse, LLC has 4 FDA 510(k) cleared medical devices. Based in New York, US.
Latest FDA clearance: Mar 2025. Active since 2018. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Xtreem Pulse, LLC Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Iuvo Consulting, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Xtreem Pulse, LLC
4 devices