meddevicedb.com FDA Device Reference

SmoothSkin Pure Unplugged (SSB3)

K240587 Class II Special
Decision Date
2024-03-29
Sponsor / Applicant
Cyden Limited

Technical Specification

510(k) Submission ID K240587
Product Code OHT
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4810
Decision Date 2024-03-29
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SmoothSkin Pure Unplugged (SSB3) received FDA 510(k) clearance under submission number K240587, sponsored by Cyden Limited. The device was reviewed via the Special premarket notification pathway and assigned to the General, Plastic Surgery review panel. The statutory decision date of record is 2024-03-29.

Classification & Regulation

This clearance is catalogued under FDA product code OHT and 21 CFR 878.4810, within the General, Plastic Surgery review panel as a Class II device.