Xtreem Pulse
FDA Regulatory Profile
Xtreem Pulse appears in FDA public data with 0 recalls, 6 510(k) clearances, 3 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on Sep 11, 2026.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 6
- Inspections
- 3
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K262861 | PureLift Pro Max | Sep 11, 2026 |
| K243587 | PureLift GLOW | Mar 6, 2025 |
| K230506 | PureLift Pro Edition | Jun 21, 2023 |
| K221443 | PureLift Pro Plus | Oct 21, 2022 |
| K190269 | PureLift | Aug 28, 2019 |
| K173483 | Pure Flow External Counter-Pulsation Device | May 30, 2018 |