ClearanceBrief
Company ยท US

Milex Products, Inc.

FDA 510(k) clearances and medical device recalls filed under this name, 1976 to 2000. Name variants (Inc, Corp, punctuation) are merged.

8510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
HHKCurette, Suction, Endometrial (And Accessories)2
HHWPessary, Vaginal2
GDFGuide, Needle, Surgical1
HHTSpatula, Cervical, Cytological1
HIRPerineometer1
KNAInstrument, Manual, Specialized Obstetric-Gynecologic1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Jun 15, 2000K001545PIPET CURET
Milex Products, Inc.
HHK
Dec 7, 1990K904774INGLAT-O-BALL
Milex Products, Inc.
HHW
Oct 10, 1990K904026INFLAT-O-BALL
Milex Products, Inc.
HHW
May 3, 1990K900903KOPANS HOOKWIRE LESION LOCALIZATION NEEDLE
Milex Products, Inc.
GDF
Jul 25, 1988K882628ENDO C BRUSH
Milex Products, Inc.
HHT
Jul 31, 1986K862410MILEX KEGEL PERINEAL EXERCISER
Milex Products, Inc.
HIR
Jun 16, 1986K861385MILEX BARTHOLIN GLAND CATHETER
Milex Products, Inc.
KNA
Oct 6, 1976K760264CURETTE, PROPOSED TIS-U-TRAP, METAL
Milex Products, Inc.
HHK

Latest recalls

DateFirm and productCodeLinked 510(k)
No recalls in this window.
Get alerts for these product codes