Thai Nippon Rubber Industry Co., Ltd. is one of 5048 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Thai Nippon Rubber Industry Co., Ltd. - FDA 510(k) Cleared Devices
6
Total
6
Cleared
0
Denied
Thai Nippon Rubber Industry Co., Ltd. has 6 FDA 510(k) cleared medical devices. Based in Durham, US.
Historical record: 6 cleared submissions from 2000 to 2015. Primary specialty: Obstetrics & Gynecology.
Browse the FDA 510(k) cleared devices submitted by Thai Nippon Rubber Industry Co., Ltd. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Thai Nippon Rubber Industry Co., Ltd.
6 devices
Cleared
Jul 30, 2015
OneTouch Lubricant Gel
Obstetrics & Gynecology
307d
Cleared
Oct 16, 2009
THAI NIPPON MALE LATEX CONDOM
Obstetrics & Gynecology
529d
Cleared
Dec 16, 2003
THAI NIPPON EXTRA STRENGTH MALE LATEX CONDOM
Obstetrics & Gynecology
90d
Cleared
Jul 20, 2001
FLAVORED MALE LATEX CONDOM
Obstetrics & Gynecology
87d
Cleared
Aug 08, 2000
'ONE TOUCH' LATEX CONDOM WITH NONOXYNOL-9
Obstetrics & Gynecology
40d
Cleared
Jan 18, 2000
LATEX CONDOM
Obstetrics & Gynecology
46d