Maquet Cardiovascular, LLC - FDA 510(k) Cleared Devices
14
Total
14
Cleared
0
Denied
Maquet Cardiovascular, LLC has 14 FDA 510(k) cleared general & plastic surgery devices. Based in San Jose, US.
Latest FDA clearance: Apr 2026. Active since 2008.
Browse the complete list of FDA 510(k) cleared general & plastic surgery devices from this manufacturer. Filter by specialty or product code using the sidebar.
14 devices
Cleared
Apr 27, 2026
Fusion Bioline Vascular Graft
Cardiovascular
266d
Cleared
May 30, 2025
Vasoview Hemopro 3 Endoscopic Vessel Harvesting System (VH-6000)
General & Plastic Surgery
38d
Cleared
Feb 26, 2025
Vasoview Hemopro 3 Power Supply
General & Plastic Surgery
68d
Cleared
Feb 27, 2024
Vasoview Hemopro 3 Endoscopic Vessel Harvesting System (VH-6000), Vasoview...
General & Plastic Surgery
81d
Cleared
Apr 15, 2020
7 mm Extended Length Endoscope
General & Plastic Surgery
271d
Cleared
Sep 17, 2019
VASOVIEW HEMOPRO Extension Cable, VASOVIEW HEMOPRO 2 Extension Cable, Bipolar...
General & Plastic Surgery
57d
Cleared
Apr 19, 2016
VASOVIEW HemoPro Endoscopic Vessel Harvesting System
General & Plastic Surgery
167d
Cleared
Feb 16, 2016
FUSION Vascular Graft
Cardiovascular
69d
Cleared
Dec 03, 2013
HARVESTING CANNULA
General & Plastic Surgery
91d
Cleared
Nov 14, 2013
FUSION VASCULAR GRAFT AND FUSION BIOLINE VASCULAR GRAFT
Cardiovascular
150d
Cleared
Sep 10, 2012
HEMASHIELD WOVEN DOUBLE VELOUR VASCULAR GRAFT MODEL M00202175XXXXX
Cardiovascular
14d
Cleared
Jun 11, 2010
VASOVIEW HEMOPRO 2 ENDOSCOPIC VESSEL HARVESTING SYSTEM
General & Plastic Surgery
36d