510(k) · Cleared
ClearedPureLift Pro Plus
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Xtreem Pulse, LLC · NFO Stimulator, Transcutaneous Electrical, Aesthetic Purposes
Cleared on Oct 21, 2022 as substantially equivalent to K190269 (Xtreem Pulse, LLC, 2019) after a 156-day review. Its family tree reaches back 3 generations to 2001. 8 later devices descend from it.
- Decided
- Oct 21, 2022
- Review
- 156 days
- Class
- Class II
- Product code
- NFO
- Recalls
- None
- Predicates
- 1
Its longest line of descent runs back 3 generations to K011935 (2001). 4 ancestors in all. 8 later devices descend from it, 6 citing it directly.
- Root · 3 generations backK011935 Rejuvenique Model #RJV10Salton, Inc. · 2001
- 2 generations backK072260 Nuface, Model NU-4003Carol Cole Company · 2007
- 1 generation backK190269 PureLiftXtreem Pulse, LLC · 2019
- This deviceK221443 PureLift Pro PlusXtreem Pulse, LLC · 2022
- Descendant · cites it directly · 2 of its ownK230506 PureLift Pro EditionXtreem Pulse · 2023
- Descendant · 2 generations on · 1 of its ownK252146 Multi-functional Facial Beauty Device ( SKB-1703,SKB-1803,SKB-1909…Shenzhen Siken 3D Technology Development Co., Ltd. · 2025
- Descendant · cites it directly · 1 of its ownK243587 PureLift GLOWXtreem Pulse, LLC · 2025
- Descendant · 2 generations on · 0 of its ownK261370 LED Light Therapy Masks (LED Face Mask Pulse (FAC06NA))Guangdong Newdermo Biotech Co., Ltd. · 2026
- Descendant · cites it directly · 0 of its ownK262861 PureLift Pro MaxXtreem Pulse, LLC · 2026
Showing 5 of 8 descendants. See all descendants
Descendants cleared per year
Most influential descendants
Showing 5 of 8 · See all- K230506PureLift Pro EditionXtreem Pulse · 2023 · cites it directly2descendants
- K252146Multi-functional Facial Beauty Device ( SKB-1703,SKB-1803,SKB-1909, SKB-2003…Shenzhen Siken 3D Technology Development Co., Ltd. · 2025 · 2 generations on1descendant
- K243587PureLift GLOWXtreem Pulse, LLC · 2025 · cites it directly1descendant
- K261370LED Light Therapy Masks (LED Face Mask Pulse (FAC06NA))Guangdong Newdermo Biotech Co., Ltd. · 2026 · 2 generations on0descendants
- K262861PureLift Pro MaxXtreem Pulse, LLC · 2026 · cites it directly0descendants
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −3 | K011935 | Rejuvenique Model #RJV10 | Salton, Inc. | 2001 | — |
| −2 | K072260 | Nuface, Model NU-4003 | Carol Cole Company | 2007 | — |
| −1 | K190269 | PureLift | Xtreem Pulse, LLC | 2019 | — |
| 0 (this device) | K221443 | PureLift Pro Plus | Xtreem Pulse, LLC | 2022 | — |
| +1 | K230506 | PureLift Pro Edition | Xtreem Pulse | 2023 | — |
| +2 | K252146 | Multi-functional Facial Beauty Device ( SKB-1703,SKB-1803,SKB-1909, SKB-2003… | Shenzhen Siken 3D Technology Development Co., Ltd. | 2025 | — |
| +1 | K243587 | PureLift GLOW | Xtreem Pulse, LLC | 2025 | — |
| +2 | K261370 | LED Light Therapy Masks (LED Face Mask Pulse (FAC06NA)) | Guangdong Newdermo Biotech Co., Ltd. | 2026 | — |
| +1 | K262861 | PureLift Pro Max | Xtreem Pulse, LLC | 2026 | — |
Other ancestors by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2005 | 1 | 0 |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2023 | 1 | 0 |
| 2025 | 3 | 0 |
| 2026 | 4 | 0 |
Sources: FDA 510(k) database (decision fields), the FDA summary (predicates and indications), FDA recall and enforcement reports, and MAUDE; processed by 510(k) Report. Verify on FDA.gov · Methodology and accuracy.
Planning a device in NFO? A 510(k) Report weighs predicate choices, recall history and review times for a new device like this one.
Top candidate predicates for a new NFO device
- #1 K233010 Beagank 4T Plusscore 28.6 · 5 generations · no Class I recall
- #2 Held for the reportin the report
- #3 Held for the reportin the report
What was it cleared against? (1)
Devices the submitter claimed this one is substantially equivalent to (*), and reference devices cited for a specific test or feature (†), as written in the FDA summary.
What descends from it? (8)
6 later devices cite it directly; ranked here by how many devices descend from each in turn.
Has anything in its family been recalled? (0 Class I)
No FDA recall names this device.
No ancestor or descendant has a Class I recall.
What does this lineage say?
- The line of descent spans 21 years and passes through 3 companies; a new generation was cleared every 6.3 years on median.
- None of the 4 ancestors has a recall.
- Of its descendants, K230506 (Xtreem Pulse, 2023) has gone furthest, with 2 descendants of its own.
How does its category compare?
All NFO devicesNFO Stimulator, Transcutaneous Electrical, Aesthetic Purposes: FDA decisions, review times, recalls and adverse event reports over 20 years. 2022, this device’s year, is highlighted.
FDA decisions per year · NFO
16in 2025
2026 to Oct 25, outlined.
Median 510(k) review, days · NFO
124in 2025
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · NFO
2in 2012
Class I (0 since 2007) Class II/III not classified
Adverse event reports per year · NFO
4in 2025
MAUDE reports naming product code NFO, not matched to any one device; reports are not rates.
View these four charts as a table
| Year | Decisions | Median 510(k) review, days | Recalls (Class I) | MAUDE reports |
|---|---|---|---|---|
| 2007 | 1 | — | 0 | 0 |
| 2008 | 3 | 550 | 0 | 0 |
| 2009 | 0 | — | 0 | 0 |
| 2010 | 0 | — | 0 | 0 |
| 2011 | 3 | 394 | 0 | 1 |
| 2012 | 3 | 160 | 2 | 0 |
| 2013 | 2 | — | 0 | 1 |
| 2014 | 2 | — | 0 | 0 |
| 2015 | 2 | — | 0 | 1 |
| 2016 | 2 | — | 0 | 5 |
| 2017 | 7 | 189 | 0 | 0 |
| 2018 | 5 | 177 | 0 | 0 |
| 2019 | 3 | 149 | 0 | 1 |
| 2020 | 2 | — | 0 | 6 |
| 2021 | 7 | 210 | 0 | 6 |
| 2022 | 2 | — | 0 | 5 |
| 2023 | 8 | 128 | 0 | 1 |
| 2024 | 5 | 109 | 0 | 4 |
| 2025 | 16 | 124 | 0 | 4 |
| 2026 | 8 | 153 | 0 | — |
What is it indicated for?
Intended for facial stimulation and indicated for-over-the counter cosmetic use.
Indications for use read by OCR from a scanned FDA summary, so letters may be misread. Check the PDF before quoting it.
https://510kreport.com/device/K221443 · printed Nov 6, 2026
Cite this page
510(k) Report. “K221443: PureLift Pro Plus.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K221443
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Record history
- FDA decision record loaded May 2, 2026
- Summary read Oct 13, 2026 (extraction version 9eaa42aa01ed)
- Lineage and recalls computed Nov 3, 2026
- Page last updated Nov 3, 2026