Unimar, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Unimar, Inc. - FDA 510(k) Cleared Devices
10
Total
9
Cleared
0
Denied
Unimar, Inc. has 9 FDA 510(k) cleared obstetrics & gynecology devices. Based in Mchenry, US.
Historical record: 9 cleared submissions from 1981 to 1994.
Browse the complete list of FDA 510(k) cleared obstetrics & gynecology devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Unimar, Inc.
10 devices
Cleared
Apr 12, 1994
KRONNER REINFORCING STYLETTE
Obstetrics & Gynecology
327d
Cleared
Oct 19, 1992
HSG TRAY
Obstetrics & Gynecology
241d
Cleared
May 01, 1991
UNI-SEM(TM)
Obstetrics & Gynecology
97d
Cleared
Dec 14, 1990
KRONNER MANIPUJECTOR
Obstetrics & Gynecology
74d
Cleared
Dec 19, 1989
HUI MINI-FLEX
Obstetrics & Gynecology
90d
Cleared
Nov 29, 1989
ASPIRETTE ENDOCERVICAL ASPIRATOR
Obstetrics & Gynecology
83d
Cleared
Aug 15, 1989
KDF-2.3
Obstetrics & Gynecology
56d
Cleared
May 11, 1989
CERVEX-BRUSH
Obstetrics & Gynecology
79d
Cleared
Mar 13, 1986
ENDOMETRIAL PIPELLE
Obstetrics & Gynecology
129d
Cleared
Mar 18, 1981
STERILE/DISPOSABLE HSG TRAY
General Hospital
43d