Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under 2 spellings of its name, each linked to the record.
As of Nov 13, 2026, FDA's public records list Xtreem Pulse, LLC with 6 510(k) clearances. The most recent is a 510(k) clearance dated Sep 11, 2026: PureLift Pro Max.
Drug approvals, 510(k) clearances, recalls and letters, 2017 to 2026 to date
A hatched bar is a year that is not over, so its count covers only part of the year.
| Sep 11, 2026 | PureLift Pro MaxK262861 · NFO | 510(k) clearances |
| Mar 6, 2025 | PureLift GLOWK243587 · NFO | 510(k) clearances |
| Jun 21, 2023 | PureLift Pro EditionK230506 · NFO | 510(k) clearances |
| Oct 21, 2022 | PureLift Pro PlusK221443 · NFO | 510(k) clearances |
| Aug 28, 2019 | PureLiftK190269 · NFO | 510(k) clearances |
| May 30, 2018 | Pure Flow External Counter-Pulsation DeviceK173483 · DRN | 510(k) clearances |
Spellings are joined only when they reduce to the same name, or a reviewed source names the same company. Sharing an FDA establishment number (FEI) is not enough: contract sites make products for many firms. Facts marked AI were labelled by a language model from the firm's FDA names; everything else comes from FDA or Wikidata. How this page is built
