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 Machida America with 8 510(k) clearances. The most recent is a 510(k) clearance dated Jan 14, 1988: MACHIDA AMERICA MODEL AC-5000 AUTOMATIC DISINFECT..
| Jan 14, 1988 | MACHIDA AMERICA MODEL AC-5000 AUTOMATIC DISINFECT.K871712 · NVE | 510(k) clearances |
| Feb 28, 1986 | MACHIDA SEMI-RIGID BRONCHOSCOPE FBS-6R-50K854581 · EOQ | 510(k) clearances |
| Jun 11, 1985 | MACHIDA FLEXIBLE NASOPHARYNGO-LARYNGOSCOPE FNS-1K844834 · EOQ | 510(k) clearances |
| May 16, 1984 | FLEXIBLE ORTHOPEDIC ENDOSCOPE ICA-1000K841087 · HRX | 510(k) clearances |
| May 13, 1982 | FLEXIBLE NASOPHARYNGO-LARYNGOSCOPE #K821181 · EQN | 510(k) clearances |
| May 13, 1982 | MODEL ENT-4L-FLEXIBLE NASOPHARYNGO-K821182 · EQN | 510(k) clearances |
| Oct 19, 1981 | MACHIDA FLEXIBLE INTUBATION SCOPE FLS-PK812734 · EQN | 510(k) clearances |
| Jul 28, 1981 | MACHIDA NASOPHARYNGO-LARYNGOSCOPEK811943 · EQN | 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
