Remington Medical, Inc. - FDA 510(k) Cleared Devices
19
Total
19
Cleared
0
Denied
Remington Medical, Inc. has 19 FDA 510(k) cleared medical devices. Based in Great Neck, US.
Latest FDA clearance: Nov 2025. Active since 1993. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Remington Medical, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Remington Medical, Inc.
19 devices
Cleared
Nov 20, 2025
VascuChek Kit, VascuChek Transceiver, VascuChek Clinical Probe, VascuChek...
Cardiovascular
153d
Cleared
Aug 30, 2024
VascuChek Kit, VascuChek Transceiver, VascuChek Clinical Probe, VascuChek...
Cardiovascular
88d
Cleared
Jan 27, 2022
VascuChek Kit, VascuChek Transceiver, VascuChek Surgical Probe, VascuChek...
Cardiovascular
248d
Cleared
Oct 07, 2021
VascuChek Kit, VascuChek Transceiver, VascuChek Clinical Probe, VascuChek...
Cardiovascular
97d
Cleared
Jul 12, 2019
Remington Medical, Inc. Automatic Cutting Needle (NAC)
General & Plastic Surgery
58d
Cleared
Jun 04, 2015
Remington Medical Inc. Tuohy Epidural Needles
Anesthesiology
120d
Cleared
May 13, 2013
REMINGTON MEDICAL CENTREFIRE 22 BIOPSY INSTRUMENT
Gastroenterology & Urology
97d
Cleared
May 19, 2005
ADAPTER CABLE
Cardiovascular
42d
Cleared
Jul 09, 2004
CORE NEEDLE BIOPSY
Gastroenterology & Urology
155d
Cleared
Aug 12, 1999
DRAINAGE BAG
Gastroenterology & Urology
182d
Cleared
Nov 03, 1998
NEEDLE GUIDE
Radiology
19d
Cleared
Sep 08, 1998
PROSTATE BIOPSY NEEDLE
Gastroenterology & Urology
60d