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 Innomed Technologies and its 1 subsidiaries with 5 510(k) clearances. The most recent is a 510(k) clearance dated Nov 5, 2009: NASAL AIRE II PEDIATRIC, MODEL 5 SIZES, MODEL TBD.
| Nov 5, 2009 | NASAL AIRE II PEDIATRIC, MODEL 5 SIZES, MODEL TBDK090804 · BZD | 510(k) clearances |
| Aug 17, 2006 | RESPCARE HYBRID NE FACE MASK, MODEL TBD,; DISPOSABLE, MODEL TBDK062019 · CBK | 510(k) clearances |
| May 4, 2005 | IT NASAL MASKK050171 · BZD | 510(k) clearances |
| Jan 14, 2004 | NASAL-AIR CRITICAL CAREK031896 · MNS | 510(k) clearances |
| Mar 21, 2003 | MODIFICATION TO NASAL-AIREK022465 · BZD | 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
