Origio A/S - FDA 510(k) Cleared Devices
14
Total
14
Cleared
0
Denied
Origio A/S has 14 FDA 510(k) cleared obstetrics & gynecology devices. Based in San Diego, US.
Historical record: 14 cleared submissions from 2010 to 2020.
Browse the complete list of FDA 510(k) cleared obstetrics & gynecology devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Origio A/S
14 devices
Cleared
Jun 25, 2020
VitriGuard
Obstetrics & Gynecology
87d
Cleared
May 04, 2018
VitriGuard
Obstetrics & Gynecology
43d
Cleared
Mar 02, 2018
ORIGIO® Handling™ without phenol red (Cat. No. 8310), ORIGIO® Handling™ with...
Obstetrics & Gynecology
98d
Cleared
Oct 13, 2017
SAGE 1-Step GM-CSF with HSA, SAGE 1-Step GM-CSF with SPS
Obstetrics & Gynecology
84d
Cleared
Mar 09, 2017
Transem and EchoGen Embryo Transfer Catheters
Obstetrics & Gynecology
279d
Cleared
Feb 16, 2017
VitriGuard
Obstetrics & Gynecology
128d
Cleared
Jul 22, 2016
ORIGIO Gradient 100, ORIGIO Gradient 90, ORIGIO Gradient 40/80, ORIGIO Sperm...
Obstetrics & Gynecology
253d
Cleared
Feb 29, 2016
BlastGen
Obstetrics & Gynecology
147d
Cleared
Jun 16, 2014
EMBRYOGEN
Obstetrics & Gynecology
126d
Cleared
May 14, 2014
ORIGIO SEQUENTIAL FERT, ORIGIO SEQUENTIAL FERT WITH PHENOL RED, ORIGIO...
Obstetrics & Gynecology
142d
Cleared
Apr 29, 2014
ORIGIO(R) SEQUENTIAL BLAST TM
Obstetrics & Gynecology
175d
Cleared
Apr 16, 2014
SAGE 1-STEP WITH HUMAN SERUM ALBUMIN, SAGE 1-STEP WITH SERUM PROTEIN SUPPLEMENTS
Obstetrics & Gynecology
133d