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 15, 2026, FDA's public records list Medtech Intl., Inc. with 6 510(k) clearances. The most recent is a 510(k) clearance dated Dec 11, 1992: CUT RESISTANT GLOVES OR SURGICAL GLOVE LINER.
| Dec 11, 1992 | CUT RESISTANT GLOVES OR SURGICAL GLOVE LINERK920876 · KGO | 510(k) clearances |
| Jan 9, 1986 | IV MATEK853843 · FLN | 510(k) clearances |
| Sep 24, 1979 | HYPERDERMIC NEEDLE WITH SENSOR #514K791462 · FMI | 510(k) clearances |
| Mar 26, 1979 | SURGICAL EYE SPONGEK790467 · EFQ | 510(k) clearances |
| Mar 26, 1979 | GAUZE & COTTON SPONGESK790389 · GDY | 510(k) clearances |
| Sep 20, 1978 | STIMULATOR, NERVE, TRANSCUTANEOUSK781157 · | 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
