meddevicedb.com FDA Device Reference

swiftPro System (SWF-SPS); Swift System (SWF-SYS)

K250718 Class II Traditional
Decision Date
2025-08-08
Sponsor / Applicant
Emblation Limited

Technical Specification

510(k) Submission ID K250718
Product Code NEY
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4400
Decision Date 2025-08-08
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

swiftPro System (SWF-SPS); Swift System (SWF-SYS) received FDA 510(k) clearance under submission number K250718, sponsored by Emblation Limited. The device was reviewed via the Traditional premarket notification pathway and assigned to the General, Plastic Surgery review panel. The statutory decision date of record is 2025-08-08.

Classification & Regulation

This clearance is catalogued under FDA product code NEY and 21 CFR 878.4400, within the General, Plastic Surgery review panel as a Class II device.