Inneuroco, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Inneuroco, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Thinline Sheath Introducer, 091 Balloon Guide Catheter, 046 Zenith Flex
9
Total
9
Cleared
0
Denied
Inneuroco, Inc. has 9 FDA 510(k) cleared medical devices. Based in Sunrise, US.
Last cleared in 2023. Active since 2016. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Inneuroco, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Inneuroco as regulatory consultant.
FDA 510(k) Regulatory Record - Inneuroco, Inc.
9 devices
Cleared
Sep 27, 2023
Thinline Sheath Introducer
Cardiovascular
58d
Cleared
Jul 29, 2022
091 Balloon Guide Catheter
Neurology
175d
Cleared
Aug 02, 2019
046 Zenith Flex
Neurology
169d
Cleared
Oct 25, 2018
074 Zenith Flex System
Neurology
156d
Cleared
Apr 19, 2018
Zenith Flex System
Neurology
275d
Cleared
Jan 26, 2018
Zenith Support, 95 cm, Zenith Support, 105 cm, Zenith Support, 115 cm
Cardiovascular
53d
Cleared
Dec 06, 2017
091 Long Sheath, 70 cm, 091 Long Sheath, 80 cm, 091 Long Sheath, 90 cm
Cardiovascular
113d
Cleared
Oct 19, 2017
065 Zenith, 074 Zenith
Cardiovascular
135d
Cleared
Sep 19, 2016
Super Distal Access (SDA)
Cardiovascular
137d