Medical device makerLabelled 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 13, 2026, FDA's public records list Medi-Spec with 8 510(k) clearances. The most recent is a 510(k) clearance dated Feb 4, 1984: LAMINARIA JAPONICA CERVICAL DILATOR.
| Date | Record | Source |
|---|---|---|
| Feb 4, 1984 | LAMINARIA JAPONICA CERVICAL DILATORK833068 · HDY | 510(k) clearances |
| Oct 26, 1981 | WHISK-RK812694 · GEE | 510(k) clearances |
| Oct 8, 1981 | UTERINE ASPIRATION CURETTES(RIGID&FLEX)K812426 · HHK | 510(k) clearances |
| Aug 4, 1980 | STERILE CAST PADDINGK801554 · HIX | 510(k) clearances |
| Apr 24, 1980 | MEDSPEC OPERATIVE OPTHALMIC KITK800404 · HMP | 510(k) clearances |
| Mar 12, 1980 | STERILE DRESSING PACKK800490 · KKX | 510(k) clearances |
| Jun 5, 1979 | CLAMP COVERSK790952 · GAD | 510(k) clearances |
| Aug 21, 1978 | DISPOSA-LOOPSK780548 · KKX | 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
