Medical Device Manufacturer · US , Morrisville , NC

Ncontact Surgical, Inc. - FDA 510(k) Cleared Devices

7 submissions · 7 cleared · Since 2006

Recent clearances: EPI-SENSE GUIDED COAGULATION DEVICE WITH VISITRAX, EPI-SENSE GUIDED COAGULATION DEVICE WITH VISITRAX, NUMERIS GUIDED COAGULATION SYSTEM WITH VISITRAX, MODELS CSK-121, -122, -123 AND -125

View 7 510(k) Devices ↓

7

Total

7

Cleared

0

Denied

FDA 510(k) Regulatory Record - Ncontact Surgical, Inc. General & Plastic Surgery ✕

1 devices

1-1 of 1

Cleared Dec 01, 2006

NCONTACT COAGULATION SYSTEM KIT

General & Plastic Surgery · 94d