Medical Device Manufacturer · US , Waterbury , CT

Northeast Scientific, Inc. - FDA 510(k) Cleared Devices

6 submissions · 6 cleared · Since 2007

6

Total

6

Cleared

0

Denied

Northeast Scientific, Inc. has 6 FDA 510(k) cleared medical devices. Based in Waterbury, US.

Latest FDA clearance: May 2025. Active since 2007. Primary specialty: Cardiovascular.

Browse the FDA 510(k) cleared devices submitted by Northeast Scientific, Inc. Filter by specialty or product code using the sidebar.

6 devices

1–6 of 6

NES Reprocessed Visions PV .018 Digital IVUS Catheter (R-86700)

K250592 · OWQ Reprocessed Intravascular Ultrasound Catheter · Cardiovascular

NES Reprocessed Eagle Eye Platinum RX Digital IVUS Catheter

K223026 · OWQ Reprocessed Intravascular Ultrasound Catheter · Cardiovascular

NES Reprocessed 0.9mm Turbo Elite Laser Atherectomy Catheter

K220171 · QTF Reprocessed Atherectomy Catheter · Cardiovascular

NES Reprocessed Visions PV .014P RX Digital IVUS Catheter

K200195 · OBJ Catheter, Ultrasound, Intravascular · Cardiovascular

NES REPROCESSED VARICOSE VEIN RF CATHETER

K090661 · NUJ Electrosurgical, Cutting & Coagulation Accessories, Laparoscopic & Endoscopic, Reprocessed · General & Plastic Surgery

NES REPROCESSED ENDOSCOPIC TROCAR

K060676 · NLM Laparoscope, General & Plastic Surgery, Reprocessed · Gastroenterology & Urology