Remington Medical, Inc. - FDA 510(k) Cleared Devices

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.

510(k) submissions have been managed by Secure BioMed Evaluations as regulatory consultant.