Innolatex Sdn. Bhd is one of 78 FDA 510(k) medical device manufacturers from Malaysia in the dataset, ranked by real submission volume.
Innolatex Sdn. Bhd - FDA 510(k) Cleared Devices
9
Total
9
Cleared
0
Denied
Innolatex Sdn. Bhd has 9 FDA 510(k) cleared medical devices. Based in Shah Alam,Selangor Darul Ehsan, MY.
Historical record: 9 cleared submissions from 2000 to 2006. Primary specialty: Obstetrics & Gynecology.
Browse the FDA 510(k) cleared devices submitted by Innolatex Sdn. Bhd Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Innolatex Sdn. Bhd
9 devices
Cleared
Feb 21, 2006
MALE NATURAL RUBBER LATEX CONDOM
Obstetrics & Gynecology
78d
Cleared
Sep 24, 2004
INNOLATEX MALE LATEX CONDOMS COLORED AND SCENTED
Obstetrics & Gynecology
79d
Cleared
Nov 09, 2001
ULTRA THICK MALE LATEX CONDOM WITH SILICONE LUBRICANT
Obstetrics & Gynecology
88d
Cleared
Nov 09, 2001
ULTRA THIN MALE LATEX CONDOM WITH SILICONE LUBRICANT
Obstetrics & Gynecology
88d
Cleared
Nov 09, 2001
DOTTED CONDOM, MALE NATURAL RUBBER LATEX CONDOM
Obstetrics & Gynecology
66d
Cleared
Nov 09, 2001
56MM CONDOM,MALE NATURAL RUBBER LATEX CONDOM
Obstetrics & Gynecology
66d
Cleared
Jun 15, 2001
MALE NATURAL RUBBER LATEX CONDOM
Obstetrics & Gynecology
80d
Cleared
Apr 27, 2001
SPERMICIDAL LUBRICATED MALE LATEX CONDOM
Obstetrics & Gynecology
98d
Cleared
Dec 19, 2000
NON-SPERMICIDAL LUBRICATED MALE LATEX CONDOM
Obstetrics & Gynecology
134d