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 Dentsply SironaLabelled 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 15, 2026, FDA's public records list Gendex Corp with 14 510(k) clearances and 1 device recall. The most recent is a device recall dated Aug 12, 2014: eXpertDC intraoral x-ray, models: eXpert DC, NA, 75 Inch reach; eXpert DC, NA, 65 Inch r….
| Aug 12, 2014 | eXpertDC intraoral x-ray, models: eXpert DC, NA, 75 Inch reach; eXpert DC, NA, 65 Inch reach; eXpert DC, CN, 55 Inch reach; eXpert DC, WW, 7Class II · Two (2) failures of the spring link components within the articulated arm assembly. The spring links broke during normal | Device recalls |
| Jun 29, 1995 | GX-PAN PANORAMIC DENTAL X-RAY SYSTEMK952598 · GEX | 510(k) clearances |
| Feb 9, 1995 | PROCESSOR, RADIOGRAPHIC-FILM, AUTOMATIC, DENTALK945682 · EGY | 510(k) clearances |
| Feb 18, 1994 | GX-770 X-RAY CONTROL, MODEL 46-404600G4K935046 · EHD | 510(k) clearances |
| Sep 29, 1993 | VISUALIX RADIOGRAPHIC IMAGE DETECTING AND PROCESSK925094 · EHD | 510(k) clearances |
| Sep 14, 1993 | ORALIX DCK931001 · EHD | 510(k) clearances |
| Jul 26, 1993 | GXP DENTAL X-RAY PROCESSORK932675 · EGN | 510(k) clearances |
| Jul 27, 1992 | ATC725, ATC525, AND AP300K922165 · IZO | 510(k) clearances |
| Apr 28, 1992 | GX-C CEPHALOMETERK920189 · EAG | 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
