Company ยท US
Xtreem Pulse, LLC
FDA 510(k) clearances and medical device recalls filed under this name, 2018 to 2026. Name variants (Inc, Corp, punctuation) are merged.
6510(k) clearances (1 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)
Product codes
Latest 510(k) clearances
| Decided | 510(k) | Device and applicant | Code |
|---|---|---|---|
| Sep 11, 2026 | K262861 | PureLift Pro Max Xtreem Pulse, LLC | NFO |
| Mar 6, 2025 | K243587 | PureLift GLOW Xtreem Pulse, LLC | NFO |
| Jun 21, 2023 | K230506 | PureLift Pro Edition Xtreem Pulse | NFO |
| Oct 21, 2022 | K221443 | PureLift Pro Plus Xtreem Pulse, LLC | NFO |
| Aug 28, 2019 | K190269 | PureLift Xtreem Pulse, LLC | NFO |
| May 30, 2018 | K173483 | Pure Flow External Counter-Pulsation Device Xtreem Pulse, LLC | DRN |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||