Medical Device Manufacturer · US , Mchenry , IL

Milex Products, Inc. - FDA 510(k) Cleared Devices

8 submissions · 8 cleared · Since 1976

Recent clearances: PIPET CURET, INGLAT-O-BALL, INFLAT-O-BALL

View 8 510(k) Devices ↓

Total

Cleared

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.

Milex Products, Inc. is one of 26109 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Milex Products, Inc.

8 devices

1-8 of 8

Cleared Jun 15, 2000

PIPET CURET

K001545 · HHK

Obstetrics & Gynecology · 28d

Cleared Dec 07, 1990

INGLAT-O-BALL

K904774 · HHW

Obstetrics & Gynecology · 46d

Cleared Oct 10, 1990

INFLAT-O-BALL

K904026 · HHW

Obstetrics & Gynecology · 41d

Cleared May 03, 1990

KOPANS HOOKWIRE LESION LOCALIZATION NEEDLE

K900903 · GDF

General & Plastic Surgery · 65d

Cleared Jul 25, 1988

ENDO C BRUSH

K882628 · HHT

Obstetrics & Gynecology · 28d

Cleared Jul 31, 1986

MILEX KEGEL PERINEAL EXERCISER

K862410 · HIR

Gastroenterology & Urology · 36d

Cleared Jun 16, 1986

MILEX BARTHOLIN GLAND CATHETER

K861385 · KNA

Obstetrics & Gynecology · 63d

Cleared Oct 06, 1976

CURETTE, PROPOSED TIS-U-TRAP, METAL

K760264 · HHK

Obstetrics & Gynecology · 77d

Milex Products, Inc. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Milex Products, Inc.

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