Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

Progeny, Inc.

FDA 510(k) & PMA Approved Devices — 5 products

Total Devices5

Categories0

Latest FDA decision

Type	Number	Device Name	Code	Date	Actions
510(k)	K090079	VIVID, MODELS 40-A0001, 40-A0004, 40-A0006	EIA	2009-05-01	View
510(k)	K070664	PROGENY IMAGING SOFTWARE, MODEL# 500-405 (6,7,8).	MUH	2007-04-26	View
510(k)	K043092	PREVA, 76IN ARM, 66IN ARM, 56IN ARM, MODELS P7017, P7016, P7015	EHD	2004-12-13	View
510(k)	K041831	PROGENY MPSE INTRAORAL DENTAL X-RAY SENSOR	MUH	2004-08-09	View
510(k)	K020070	JB-70 INTRAORAL X-RAY SYSTEM, MODELS 30-A0001/A0002	EHD	2002-02-01	View

↑