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 Resonance Innovations with 8 510(k) clearances. The most recent is a 510(k) clearance dated Dec 5, 2014: Siemens 3.0T PROCURE Array Coil.
| Dec 5, 2014 | Siemens 3.0T PROCURE Array CoilK142676 · MOS | 510(k) clearances |
| Oct 23, 2014 | Siemens 3.0 Blanket Array CoilK142755 · MOS | 510(k) clearances |
| May 12, 2014 | 1.5T PROCURE ARRAY COIL, 3.0T PROCURE ARRAY COILK140606 · MOS | 510(k) clearances |
| Feb 26, 2014 | ST SENSE NV 8 ARRAY COILK140282 · MOS | 510(k) clearances |
| Jan 27, 2014 | 1.5T ORBIT AND MANDIBLE ARRAY, 3.0T ORBIT AND MANDIBLE ARRAYK133986 · MOS | 510(k) clearances |
| May 20, 2013 | 3T DISTAL COIL, 3T ELBOW COIL, 3T LONG BONE COILK130457 · MOS | 510(k) clearances |
| May 25, 2006 | 3.0T PEDIATRIC HEAD AND SPINE ARRAY, MODEL 808GE3000K061170 · MOS | 510(k) clearances |
| Mar 31, 2006 | 1.5T PEDIATRIC HEAD AND SPINE ARRAY MODELK060689 · MOS | 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
