Milex Products, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Milex Products, Inc. - FDA 510(k) Cleared Devices
8
Total
8
Cleared
0
Denied
Milex Products, Inc. has 8 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 8 cleared submissions from 1976 to 2000. Primary specialty: Obstetrics & Gynecology.
Browse the FDA 510(k) cleared devices submitted by Milex Products, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Milex Products, Inc.
8 devices
Cleared
Jun 15, 2000
PIPET CURET
Obstetrics & Gynecology
28d
Cleared
Dec 07, 1990
INGLAT-O-BALL
Obstetrics & Gynecology
46d
Cleared
Oct 10, 1990
INFLAT-O-BALL
Obstetrics & Gynecology
41d
Cleared
May 03, 1990
KOPANS HOOKWIRE LESION LOCALIZATION NEEDLE
General & Plastic Surgery
65d
Cleared
Jul 25, 1988
ENDO C BRUSH
Obstetrics & Gynecology
28d
Cleared
Jul 31, 1986
MILEX KEGEL PERINEAL EXERCISER
Gastroenterology & Urology
36d
Cleared
Jun 16, 1986
MILEX BARTHOLIN GLAND CATHETER
Obstetrics & Gynecology
63d
Cleared
Oct 06, 1976
CURETTE, PROPOSED TIS-U-TRAP, METAL
Obstetrics & Gynecology
77d