New Wave Surgical Corporation is one of 25260 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
New Wave Surgical Corporation - FDA 510(k) Cleared Devices
Recent clearances: DEFOGGING HEATED ENDOSCOPE LENS PROTECTOR (DHELP)
1
Total
1
Cleared
0
Denied
New Wave Surgical Corporation has 1 FDA 510(k) cleared medical devices. Based in Great Neck, US.
Historical record: 1 cleared submissions from 2006 to 2006. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by New Wave Surgical Corporation Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Citech as regulatory consultant.
FDA 510(k) Regulatory Record - New Wave Surgical Corporation
1 devices