Milex Products, Inc.
Milex Products, Inc. appears in FDA public data with 0 recalls, 8 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on June 15, 2000.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 8
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K001545 | PIPET CURET | June 15, 2000 |
| K904774 | INGLAT-O-BALL | December 7, 1990 |
| K904026 | INFLAT-O-BALL | October 10, 1990 |
| K900903 | KOPANS HOOKWIRE LESION LOCALIZATION NEEDLE | May 3, 1990 |
| K882628 | ENDO C BRUSH | July 25, 1988 |
| K862410 | MILEX KEGEL PERINEAL EXERCISER | July 31, 1986 |
| K861385 | MILEX BARTHOLIN GLAND CATHETER | June 16, 1986 |
| K760264 | CURETTE, PROPOSED TIS-U-TRAP, METAL | October 6, 1976 |