Nemoto Kyorindo Co., Ltd. is one of 136 FDA 510(k) medical device manufacturers from Japan in the dataset, ranked by real submission volume.
Nemoto Kyorindo Co., Ltd. - FDA 510(k) Cleared Devices
Recent clearances: Disposable Syringe (Kit), PRESS DUO elite, PRESS DUO elite AG, DUAL SHOT ALPHA 7
8
Total
8
Cleared
0
Denied
Nemoto Kyorindo Co., Ltd. has 8 FDA 510(k) cleared medical devices. Based in Tokyo, JP.
Latest FDA clearance: Aug 2024. Active since 2005. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Nemoto Kyorindo Co., Ltd. Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Tuv Rheinland of North America, Inc. and Third Party Review Group, LLC.
FDA 510(k) Regulatory Record - Nemoto Kyorindo Co., Ltd.
8 devices
Cleared
Aug 27, 2024
Disposable Syringe (Kit)
General Hospital
29d
Cleared
Feb 07, 2018
PRESS DUO elite, PRESS DUO elite AG
Cardiovascular
93d
Cleared
Jun 30, 2014
DUAL SHOT ALPHA 7
Cardiovascular
256d
Cleared
Oct 29, 2010
REMPRESS AND ANGIOGRAPHY CONTRAST DELIVERY SYSTEM REMPRESS
Cardiovascular
403d
Cleared
May 21, 2010
SONIC SHOT GX
Radiology
344d
Cleared
Dec 19, 2007
DUAL SHOT ALPHA
Cardiovascular
182d
Cleared
Aug 18, 2006
CONTRAST DELIVERY SYSTEM - DUAL SHOT ALPHA
Cardiovascular
18d
Cleared
Oct 17, 2005
DUAL SHOT - CONTRAST DELIVERY SYSTEM
Cardiovascular
21d