Milex Products, Inc.: FDA filings under this applicant name
FDA lists 8 510(k) clearances under the applicant name “Milex Products, Inc.” (first 1976, latest 2000), across 6 product codes in 3 review panels. Median 510(k) review time under this name: 44 days. Related companies, subsidiaries and acquired businesses that file under other applicant names are counted on their own pages, not here.
510(k) clearances per year
| Year | Clearances | Median review days |
|---|---|---|
| 2012 | 0 | — |
| 2013 | 0 | — |
| 2014 | 0 | — |
| 2015 | 0 | — |
| 2016 | 0 | — |
| 2017 | 0 | — |
| 2018 | 0 | — |
| 2019 | 0 | — |
| 2020 | 0 | — |
| 2021 | 0 | — |
| 2022 | 0 | — |
| 2023 | 0 | — |
| 2024 | 0 | — |
| 2025 | 0 | — |
| 2026 | 0 | — |
Top product codes
| Product code | Device | Submissions | 510(k) clearances |
|---|---|---|---|
| HHK | Curette, Suction, Endometrial (And Accessories) | 2 | 2 |
| HHW | Pessary, Vaginal | 2 | 2 |
| GDF | Guide, Needle, Surgical | 1 | 1 |
| HHT | Spatula, Cervical, Cytological | 1 | 1 |
| HIR | Perineometer | 1 | 1 |
| KNA | Instrument, Manual, Specialized Obstetric-Gynecologic | 1 | 1 |
Review panels
Most recent Milex Products, Inc. 510(k) clearances
| 510(k) | Device | Product code | Decision date | Review days |
|---|---|---|---|---|
| K001545 | PIPET CURET | HHK | 2000-06-15 | 28 |
| K904774 | INGLAT-O-BALL | HHW | 1990-12-07 | 46 |
| K904026 | INFLAT-O-BALL | HHW | 1990-10-10 | 41 |
| K900903 | KOPANS HOOKWIRE LESION LOCALIZATION NEEDLE | GDF | 1990-05-03 | 65 |
| K882628 | ENDO C BRUSH | HHT | 1988-07-25 | 28 |
| K862410 | MILEX KEGEL PERINEAL EXERCISER | HIR | 1986-07-31 | 36 |
| K861385 | MILEX BARTHOLIN GLAND CATHETER | KNA | 1986-06-16 | 63 |
| K760264 | CURETTE, PROPOSED TIS-U-TRAP, METAL | HHK | 1976-10-06 | 77 |
Recalls
openFDA lists no recalls under a recalling firm named Milex Products, Inc..
Recalling firms are matched to this applicant name by name only (same normalization), so related entities that recall under another name are not counted. A recall count says nothing about how safe one company's devices are compared with another's.
Frequently asked questions
How many FDA 510(k) clearances are listed under Milex Products, Inc.?
FDA lists 8 510(k) clearances under the applicant name “Milex Products, Inc.” (first 1976, latest 2000), across 6 product codes in 3 review panels. Filings under other applicant names, such as subsidiaries, are not included.
How long has FDA taken to clear 510(k)s filed by Milex Products, Inc.?
The median time from FDA receipt to decision across 510(k)s cleared under the name Milex Products, Inc. is 44 days.
Which FDA product codes appear under Milex Products, Inc.?
The most frequent FDA product codes under this applicant name are HHK (Curette, Suction, Endometrial (And Accessories), 2); HHW (Pessary, Vaginal, 2); GDF (Guide, Needle, Surgical, 1).
Next steps
- See all 8 Milex Products, Inc. clearances with predicates and recalls
- Run predicate analysis for product code HHK, Milex Products, Inc.'s most frequent
Data from openFDA (510(k), PMA, De Novo, device recalls), ClinicalTrials.gov and SEC company tickers. Each page covers one FDA applicant name, with punctuation and legal suffixes removed; filings under other names are not included. Review days run from FDA receipt to decision. Not regulatory advice. Report an error in this data.