# K243587: PureLift GLOW

- Pathway: 510(k) (Traditional)
- Applicant: Xtreem Pulse, LLC
- Decided: Mar 6, 2025 after 106 days
- Product code: NFO (Stimulator, Transcutaneous Electrical, Aesthetic Purposes)
- Device class: 2
- Regulation: 21 CFR 882.5890
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 17 generations back to K943450 (1995). 134 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 136 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K221443: PureLift Pro Plus, Xtreem Pulse, LLC (2022) Summary page 5.
- K223482: reVive Light Therapy® Wrinkle and Acne LED Device, Led Technologies, Inc. (2022) Summary page 5.
- K201782: NuFace Trinity Plus Device, Carol Cole Company Dba Nuface (2021) Summary page 5.

## Most influential descendants
- K261370: LED Light Therapy Masks (LED Face Mask Pulse (FAC06NA)) (2026), 0 descendants of its own

## Indications for use
PureLift GLOW is intended for facial and neck stimulation, treatment of wrinkles, treatment of mild to moderate inflammatory acne, and indicated for over-the-counter cosmetic use.

Source page: https://510kreport.com/device/K243587
Methodology: https://510kreport.com/methodology