meddevicedb.com FDA Device Reference

Nisus ONE Negative Pressure Wound Therapy System (OCMPP-100)

K243187 Class II Traditional
Decision Date
2025-06-27
Sponsor / Applicant
Cork Medical

Technical Specification

510(k) Submission ID K243187
Product Code OMP
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4780
Decision Date 2025-06-27
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Nisus ONE Negative Pressure Wound Therapy System (OCMPP-100) received FDA 510(k) clearance under submission number K243187, sponsored by Cork Medical. 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 2025-06-27.

Classification & Regulation

This clearance is catalogued under FDA product code OMP and 21 CFR 878.4780, within the General, Plastic Surgery review panel as a Class II device.