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., part of Microaire Surgical InstrumentsLabelled 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 Microaire with 3 510(k) clearances. The most recent is a 510(k) clearance dated Mar 18, 1992: MICROAIRE MODEL 2600.
| Mar 18, 1992 | MICROAIRE MODEL 2600K915670 · GEF | 510(k) clearances |
| Aug 16, 1991 | MICRO-AIRE ARTHROS SURG BLADES-VARIOUS DYS PROD NOK912205 · HRX | 510(k) clearances |
| Aug 16, 1991 | MICRO-AIRE ARTHROS SURG BLADES-VARIOUS CO PROD NO.K912206 · HRX | 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
