Not currently registered with FDA under this name

Progeny, Inc.

Lincolnshire, IL, United States. Named as applicant on 5 dental 510(k) clearances between 2002 and 2009. No establishment is registered with FDA under this exact name today.

Device types listed: 0
Brands and models: 0
510(k) clearances: 52002–2009
Markets registered in: 21 registrations outside the US
Establishments: 0—

510(k) clearances per year, 2000–2026

Registered in 2 markets

Where regulators' registries name Progeny, Inc. as the manufacturer or the registration holder of a device.

All markets

RegisteredHome: United StatesOne marker per market

Market	Regulator	Named as	Name on the registry	Registrations	Issued	Records
United States	FDA	Applicant	Progeny, Inc.	5 clearances	2002–2009	Below
South Korea	MFDS	Manufacturer	Progeny Inc	1	2005–2005	Pure Global AI

Outside the US the count is of all the company's device registrations in that market, dental or not · matched by company name and country · registry data read 12 Nov 2026

510(k) clearances

Clearances on which FDA names Progeny, Inc. as the applicant.

Decided	510(k)	Device	Device type
1 May 2009	K090079	VIVID, MODELS 40-A0001, 40-A0004, 40-A0006	EIA Operative Dental Unit
26 Apr 2007	K070664	PROGENY IMAGING SOFTWARE, MODEL# 500-405 (6,7,8).	MUH Digital Extraoral Source X-Ray System
13 Dec 2004	K043092	PREVA, 76IN ARM, 66IN ARM, 56IN ARM, MODELS P7017, P7016, P7015	EHD Extraoral with Timer X-Ray Unit
9 Aug 2004	K041831	PROGENY MPSE INTRAORAL DENTAL X-RAY SENSOR	MUH Digital Extraoral Source X-Ray System
1 Feb 2002	K020070	JB-70 INTRAORAL X-RAY SYSTEM, MODELS 30-A0001/A0002	EHD Extraoral with Timer X-Ray Unit

Some of these clearances are listed with FDA today by another company: Midmark Corporation (2).

Sources

FDA 510(k) premarket notification file. FDA data as of 2 Nov 2026; snapshot 12 Nov 2026. The location shown is the address on FDA's record of the most recent filing, which can be a US agent.