meddevicedb.com FDA Device Reference

Lipocosm Harmonic System

K251944 Class II Traditional
Decision Date
2026-06-08
Sponsor / Applicant
Lipocosm, LLC

Technical Specification

510(k) Submission ID K251944
Product Code QPB
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.5040
Decision Date 2026-06-08
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Lipocosm Harmonic System received FDA 510(k) clearance under submission number K251944, sponsored by Lipocosm, LLC. 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 2026-06-08.

Classification & Regulation

This clearance is catalogued under FDA product code QPB and 21 CFR 878.5040, within the General, Plastic Surgery review panel as a Class II device.