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 Progeny with 5 510(k) clearances. The most recent is a 510(k) clearance dated May 1, 2009: VIVID, MODELS 40-A0001, 40-A0004, 40-A0006.
| Date | Record | Source |
|---|---|---|
| May 1, 2009 | VIVID, MODELS 40-A0001, 40-A0004, 40-A0006K090079 · EIA | 510(k) clearances |
| Apr 26, 2007 | PROGENY IMAGING SOFTWARE, MODEL# 500-405 (6,7,8).K070664 · MUH | 510(k) clearances |
| Dec 13, 2004 | PREVA, 76IN ARM, 66IN ARM, 56IN ARM, MODELS P7017, P7016, P7015K043092 · EHD | 510(k) clearances |
| Aug 9, 2004 | PROGENY MPSE INTRAORAL DENTAL X-RAY SENSORK041831 · MUH | 510(k) clearances |
| Feb 1, 2002 | JB-70 INTRAORAL X-RAY SYSTEM, MODELS 30-A0001/A0002K020070 · EHD | 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
