Nihon Kohden Orangemed, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Nihon Kohden Orangemed, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Nihon Kohden NKV-440 Ventilator System, Nihon Kohden NKV-330 Ventilator System, Nihon Kohden NKV-550 Series Ventilator System
4
Total
4
Cleared
0
Denied
Nihon Kohden Orangemed, Inc. has 4 FDA 510(k) cleared medical devices. Based in Santa Ana, US.
Last cleared in 2023. Active since 2018. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by Nihon Kohden Orangemed, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Nihon Kohden Orangemed, Inc.
4 devices
Cleared
May 31, 2023
Nihon Kohden NKV-440 Ventilator System
Anesthesiology
272d
Cleared
Jul 01, 2022
Nihon Kohden NKV-330 Ventilator System
Anesthesiology
240d
Cleared
Jan 10, 2020
Nihon Kohden NKV-550 Series Ventilator System
Anesthesiology
137d
Cleared
Dec 07, 2018
Nihon Kohden NKV-550 Series Ventilator System
Anesthesiology
163d