Waismed, Ltd. is one of 472 FDA 510(k) medical device manufacturers from Israel in the dataset, ranked by real submission volume.
Waismed, Ltd. - FDA 510(k) Cleared Devices
Recent clearances: NIO+ Adult, NIO-I, NIO-P
7
Total
7
Cleared
0
Denied
Waismed, Ltd. has 7 FDA 510(k) cleared medical devices. Based in Ra'Ananna, IL.
Last cleared in 2021. Active since 1998. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Waismed, Ltd. Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Hogan Lovells US LLP and Talmed , Ltd..
FDA 510(k) Regulatory Record - Waismed, Ltd.
7 devices
Cleared
Jul 22, 2021
NIO+ Adult
General Hospital
28d
Cleared
Oct 07, 2019
NIO-I
General Hospital
217d
Cleared
Jun 23, 2016
NIO-P
General Hospital
92d
Cleared
Aug 28, 2014
NIO -INTRAOSSEOUS DEVICE
General Hospital
28d
Cleared
Dec 22, 2006
BONE INJECTION GUN (B.I.G.)
General Hospital
85d
Cleared
Oct 11, 2002
BONE INJECTION GUN (B.I.G.) FOR PEDIATRICS, MODEL 1ST
General Hospital
79d
Cleared
Nov 17, 1998
BONE INJECTION GUN (B.I.G.) DEVICE
General Hospital
175d