Novo Nordisk, Inc. - FDA 510(k) Cleared Devices
14
Total
14
Cleared
0
Denied
Novo Nordisk, Inc. has 14 FDA 510(k) cleared general hospital devices. Based in Princeton, US.
Last cleared in 2023. Active since 2005.
Browse the complete list of FDA 510(k) cleared general hospital devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Novo Nordisk, Inc.
14 devices
Cleared
Aug 25, 2023
NovoFine® Plus
General Hospital
116d
Cleared
Jun 23, 2021
NovoFine
General Hospital
142d
Cleared
Dec 19, 2020
NovoFine Plus 32G Tip x 4 mm
General Hospital
151d
Cleared
Dec 17, 2018
NovoPen Echo Dial-A-Dose Insulin Delivery Device (Pen Injector)
General Hospital
104d
Cleared
Jan 17, 2018
NovoFine 32G Tip (0.23/0.25) x 6 mm ETW (extra thin wall)
General Hospital
65d
Cleared
Oct 18, 2016
NovoPen Echo
General Hospital
29d
Cleared
Jul 31, 2015
NovoPen Echo Dial-A-Dose Insulin Delivery Device (Pen Injector)
General Hospital
121d
Cleared
May 21, 2014
NOVOFINE PLUS 32G 4 MM
General Hospital
163d
Cleared
Aug 15, 2013
NOVOPEN ECHO, A DIAL A DOSE INSULIN DELIVERY PEN
General Hospital
251d
Cleared
Jun 18, 2010
NOVOTWIST NEEDLE, MODELS 30G * 8MM (1/3) 32 G TIP * 5 MM(1/5')
General Hospital
260d
Cleared
Feb 01, 2010
FLEXPEN NEEDLE
General Hospital
381d
Cleared
Nov 21, 2006
FLEXPEN NEEDLE
General Hospital
88d