Earlysense, Ltd. is one of 267 FDA 510(k) medical device manufacturers from Israel in the dataset, ranked by real submission volume.
Earlysense, Ltd. - FDA 510(k) Cleared Devices
Recent clearances: EarlySense Bed Sensing Unit
12
Total
12
Cleared
0
Denied
Earlysense, Ltd. has 12 FDA 510(k) cleared medical devices. Based in Tel Aviv, IL.
Historical record: 12 cleared submissions from 2007 to 2018. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by Earlysense, Ltd. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Earlysense, Ltd.
12 devices
Cleared
Jan 04, 2018
EarlySense Bed Sensing Unit
Anesthesiology
198d
Cleared
May 06, 2016
EarlySense Insight Sytem
Anesthesiology
217d
Cleared
Aug 31, 2015
EarlySense Central Display Station (CDS)
Cardiovascular
138d
Cleared
Jun 13, 2014
CHAIR SENSING UNIT FOR EARLYSENSE SYSTEM
Anesthesiology
196d
Cleared
Dec 18, 2013
EARLYSENSE
Anesthesiology
218d
Cleared
Sep 10, 2012
EARLYSENSE CENTRAL DISPLAY SYSTEM
Cardiovascular
74d
Cleared
Jun 08, 2012
EARLYSENSE (EVERON) SYSTEM
Anesthesiology
114d
Cleared
Apr 19, 2011
EVERON CENTRAL DISPLAY STATION (CDS)
Cardiovascular
55d
Cleared
Aug 06, 2010
EVERON CENTRAL DISPLAY STATION - CDS, MODEL VERSION 1.0.0
Cardiovascular
175d
Cleared
May 24, 2010
EVERON 1.0
Anesthesiology
320d
Cleared
Mar 25, 2009
EVERON
Anesthesiology
210d
Cleared
Nov 15, 2007
EARLYSENSE ES-16 SYSTEM
Anesthesiology
280d