Ssl Americas is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Ssl Americas - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Ssl Americas has 5 FDA 510(k) cleared medical devices. Based in Norcross, US.
Historical record: 5 cleared submissions from 2004 to 2008. Primary specialty: Obstetrics & Gynecology.
Browse the FDA 510(k) cleared devices submitted by Ssl Americas Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Ssl Americas
5 devices
Cleared
May 07, 2008
DUREX PLAY TINGLING AQUEOUS BASED LUBRICANT
Obstetrics & Gynecology
271d
Cleared
Apr 01, 2008
DUREX PLAY SOFT & SENSUAL LUBRICANT
Obstetrics & Gynecology
292d
Cleared
Jan 27, 2006
DUREX MALE COLORED LATEX CONDOMS WITH SCENTED LUBRICANTS
Obstetrics & Gynecology
98d
Cleared
Feb 17, 2005
DUREX MALE LATEX CONDOM WITH WARMING LUBRICANT
Obstetrics & Gynecology
113d
Cleared
Apr 27, 2004
DUREX STUDDED/RIBBED LUBRICATED LATEX CONDOM
Obstetrics & Gynecology
91d