PureLift Pro Max
K-Number: K262861 · 2026-09-11
Device Summary
Frequently Asked Questions
What is the PureLift Pro Max?
PureLift Pro Max is a medical device that received FDA 510(k) clearance on 2026-09-11. The listed applicant is Xtreem Pulse, LLC. The 510(k) number is K262861.
When did PureLift Pro Max receive FDA 510(k) clearance?
PureLift Pro Max received FDA 510(k) clearance on 2026-09-11, under 510(k) number K262861.
Who is the listed applicant for PureLift Pro Max?
The FDA 510(k) record lists Xtreem Pulse, LLC as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PureLift Pro Max?
The FDA product code for PureLift Pro Max is NFO.
Other records listing Xtreem Pulse, LLC as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: NFO)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.