Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under 2 spellings of its name, each linked to the record.
As of Nov 14, 2026, FDA's public records list E-Woo Technology Co., Ltd. with 8 510(k) clearances. The most recent is a 510(k) clearance dated Aug 9, 2010: DIGITAL FLAT PANEL X-RAY DETECTOR, MODEL XMARU 1717.
| Aug 9, 2010 | DIGITAL FLAT PANEL X-RAY DETECTOR, MODEL XMARU 1717K091090 · MQB | 510(k) clearances |
| Dec 2, 2009 | MEDICAL IMAGE PROCESSING UNIT, MODEL EZSENSORK090526 · MUH | 510(k) clearances |
| Oct 9, 2009 | COMPUTED TOMOGRAPHY X-RAY SYSTEM, MODEL PICASSO-DUOK090991 · JAK | 510(k) clearances |
| Apr 30, 2009 | COMPUTED TOMOGRAPHY X-RAY SYSTEM, PAX-REVE3DK090171 · OAS | 510(k) clearances |
| Oct 31, 2008 | MASTER3DSK082410 · OAS | 510(k) clearances |
| Aug 21, 2008 | ANYRAY PORTABLE X-RAY SYSTEMK081899 · EHD | 510(k) clearances |
| Aug 21, 2008 | PICASSO MASTER, ECT AND MASTER 3DK081847 · JAK | 510(k) clearances |
| Apr 5, 2007 | DENTAL DIGITAL PANORAMIC/3D IMAGING SYSTEMK070658 · JAK | 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
