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 Med-Tech Development Corp. with 5 510(k) clearances. The most recent is a 510(k) clearance dated Mar 28, 1986: SAPPHIRE BLADE SURGICAL KNIFE.
| Mar 28, 1986 | SAPPHIRE BLADE SURGICAL KNIFEK860852 · HNN | 510(k) clearances |
| Feb 13, 1986 | DIAMOND BLADE MICROMETER KNIFEK860332 · HNN | 510(k) clearances |
| Feb 12, 1986 | DISPOSABLE SURGICAL KNIFEK860331 · HNN | 510(k) clearances |
| Feb 12, 1986 | FYODOROV RADIAL KERATOTOMY MARKER SETK860329 · HHR | 510(k) clearances |
| Feb 12, 1986 | MAKLAKOV STYLE TONOMETERK860330 · HKY | 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
