Not currently registered with FDA under this name

Fischer Imaging Corp.

Denver, CO, United States. Named as applicant on 1 dental 510(k) clearance between 1993 and 1993. No establishment is registered with FDA under this exact name today.

Device types listed: 0
Brands and models: 0
510(k) clearances: 11993–1993
Markets registered in: 210 registrations outside the US
Establishments: 0—

510(k) clearances per year, 1990–2026

Registered in 2 markets

Where regulators' registries name Fischer Imaging Corp. 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	Fischer Imaging Corp.	1 clearances	1993–1993	Below
Taiwan	TFDA	Manufacturer	FISCHER IMAGING CORPORATION.	10	1986–1991	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 Fischer Imaging Corp. as the applicant.

Decided	510(k)	Device	Device type
30 Mar 1993	K926575	MAMMOTEST PRODUCT, MODIFICATION	EHD Extraoral with Timer X-Ray Unit

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.