Nidacon International AB is one of 5134 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Nidacon International AB - FDA 510(k) Cleared Devices
12
Total
12
Cleared
0
Denied
Nidacon International AB has 12 FDA 510(k) cleared obstetrics & gynecology devices. Based in Deer Field, US.
Historical record: 12 cleared submissions from 1998 to 2014.
Browse the complete list of FDA 510(k) cleared obstetrics & gynecology devices from this manufacturer. Filter by specialty or product code using the sidebar.
Nidacon International AB — FDA 510(k) Products and Clearance History
12 devices
Cleared
Feb 20, 2014
PROINSERT
Obstetrics & Gynecology
303d
Cleared
Jun 15, 2010
VITRIBLAST, THERMOBLAST, MODEL VB-010, TB-010
Obstetrics & Gynecology
336d
Cleared
Nov 08, 2002
SPERM CRYOPROTEC
Obstetrics & Gynecology
44d
Cleared
Aug 28, 2002
SPERMASSIST
Obstetrics & Gynecology
34d
Cleared
Aug 10, 2001
SPERMCATCH
Obstetrics & Gynecology
78d
Cleared
Aug 03, 2001
NIDOIL
Obstetrics & Gynecology
28d
Cleared
Jul 12, 2001
PURESPERM BUFFER
Obstetrics & Gynecology
49d
Cleared
Jun 28, 2001
READYSWIM
Obstetrics & Gynecology
57d
Cleared
Nov 21, 2000
PURESPERM WASH
Obstetrics & Gynecology
90d
Cleared
Nov 20, 2000
PURESPERM 40 AND PURESPERM 80
Obstetrics & Gynecology
89d
Cleared
Jan 14, 1999
MODIFICATION OF PURESPERM
Obstetrics & Gynecology
55d
Cleared
Jun 23, 1998
PURESPERM
Obstetrics & Gynecology
112d