Unidus Corp. is one of 351 FDA 510(k) medical device manufacturers from South Korea in the dataset, ranked by real submission volume.
Unidus Corp. - FDA 510(k) Cleared Devices
7
Total
7
Cleared
0
Denied
Unidus Corp. has 7 FDA 510(k) cleared medical devices. Based in Seoul, Korea, KR.
Historical record: 7 cleared submissions from 1989 to 2007. Primary specialty: Obstetrics & Gynecology.
Browse the FDA 510(k) cleared devices submitted by Unidus Corp. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Unidus Corp.
7 devices
Cleared
Nov 15, 2007
UNIDUS MAGNUM MALE LATEX CONDOM
Obstetrics & Gynecology
49d
Cleared
Dec 23, 2003
LONG LOVE CONDOM
Obstetrics & Gynecology
43d
Cleared
Dec 13, 2002
UNIDUS MALE LATEX CONDOM (YELLOW, PINK, GREEN & BLACK)
Obstetrics & Gynecology
85d
Cleared
Dec 13, 2002
UNIDUS MALE LATEX CONDOM (WITH COLOR AND FLAVORING)
Obstetrics & Gynecology
81d
Cleared
Dec 13, 2002
UNDUS MALE LATEX CONDOM (WITH FLAVORING)
Obstetrics & Gynecology
81d
Cleared
Dec 12, 2002
UNIDUS MALE LATEX CONDOM
Obstetrics & Gynecology
90d
Cleared
Apr 11, 1989
SKIN ANGEL BRAND (PATIENT EXAM GLOVES - LATEX)
General Hospital
15d