# K250341: Sensilift Pro (ST300XXYYZZZ)

- Pathway: 510(k) (Traditional)
- Applicant: El Global Trade, Ltd.
- Decided: Jan 6, 2026 after 334 days
- Product code: PAY (Over-The-Counter Radiofrequency Coagulation Device For Wrinkle Reduction)
- Device class: 2
- Regulation: 21 CFR 878.4420
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 21 generations back to K943450 (1995). 96 ancestors in all.
No later device cites it as a predicate yet.
0 of 97 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K170499: sensiLift, El Global Trade, Ltd. (2017) Summary page 5.
- K220322: Pollogen STOP U Model UXV Device, Pollogen, Ltd. (2023) Summary page 5.

## Indications for use
The sensilift Pro is an over-the-counter home use device intended for non-invasive treatment of mild to moderate facial wrinkles for adults who have Fitzpatrick Skin Types I-IV.

Source page: https://510kreport.com/device/K250341
Methodology: https://510kreport.com/methodology