Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in United StatesLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under its name, each linked to the record.
As of Nov 15, 2026, FDA's public records list Milex Products, Inc. with 8 510(k) clearances. The most recent is a 510(k) clearance dated Jun 15, 2000: PIPET CURET.
| Jun 15, 2000 | PIPET CURETK001545 · HHK | 510(k) clearances |
| Dec 7, 1990 | INGLAT-O-BALLK904774 · HHW | 510(k) clearances |
| Oct 10, 1990 | INFLAT-O-BALLK904026 · HHW | 510(k) clearances |
| May 3, 1990 | KOPANS HOOKWIRE LESION LOCALIZATION NEEDLEK900903 · GDF | 510(k) clearances |
| Jul 25, 1988 | ENDO C BRUSHK882628 · HHT | 510(k) clearances |
| Jul 31, 1986 | MILEX KEGEL PERINEAL EXERCISERK862410 · HIR | 510(k) clearances |
| Jun 16, 1986 | MILEX BARTHOLIN GLAND CATHETERK861385 · KNA | 510(k) clearances |
| Oct 6, 1976 | CURETTE, PROPOSED TIS-U-TRAP, METALK760264 · HHK | 510(k) clearances |
Spellings are joined only when they reduce to the same name, or a reviewed source names the same company. Sharing an FDA establishment number (FEI) is not enough: contract sites make products for many firms. Facts marked AI were labelled by a language model from the firm's FDA names; everything else comes from FDA or Wikidata. How this page is built
