Spectrum Vascular is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Spectrum Vascular - FDA 510(k) Cleared Devices
Recent clearances: Arterial Pressure Monitoring Set/Tray, BioFlo Hybrid PICC with ENDEXO Technology and PASV Valve Technology, Intraosseous Infusion Needles
5
Total
5
Cleared
0
Denied
Spectrum Vascular has 5 FDA 510(k) cleared medical devices. Based in White Plains, US.
Latest FDA clearance: Jun 2026. Active since 2024. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Spectrum Vascular Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Spectrum Vascular
5 devices
Cleared
Jun 26, 2026
Arterial Pressure Monitoring Set/Tray
Cardiovascular
56d
Cleared
Mar 25, 2026
Arterial Pressure Monitoring Set/Tray
Cardiovascular
85d
Cleared
Dec 16, 2025
BioFlo Hybrid PICC with ENDEXO Technology and PASV Valve Technology
General Hospital
139d
Cleared
Jul 30, 2025
Intraosseous Infusion Needles
General Hospital
142d
Cleared
Nov 27, 2024
SV Spectrum MRC Central Venous Catheter
General Hospital
218d