Not currently registered with FDA under this name

Eastman Kodak Company

Rochester, NY, United States. Named as applicant on 3 dental 510(k) clearances between 1997 and 2006. No establishment is registered with FDA under this exact name today.

Device types listed
0
Brands and models
0
510(k) clearances
31997–2006
Markets registered in
360 registrations outside the US
Establishments
0—
1997: 12004: 12006: 11990200020102020

510(k) clearances per year, 1990–2026

Registered in 3 markets

Where regulators' registries name Eastman Kodak Company as the manufacturer or the registration holder of a device.

All markets
United States: 3 clearancesSouth Korea: 54 registrationsTaiwan: 6 registrations
RegisteredHome: United StatesOne marker per market
MarketRegulatorNamed asName on the registryRegistrationsIssuedRecords
United StatesFDAApplicantEastman Kodak Company3 clearances1997–2006Below
South KoreaMFDSManufacturerEastman Kodak CompanyEastman Kodak Company. · Eastman kodak Company541999–2006Pure Global AI
TaiwanTFDAManufacturerEASTMAN KODAK COMPANY61980–2006Pure 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 Eastman Kodak Company as the applicant.

Decided510(k)DeviceDevice type
8 Feb 2006K060079KODAK MODEL CR-7400 DIGITAL RADIOGRAPHY SYSTEMMUH Digital Extraoral Source X-Ray System
7 Apr 2004K040556TROPHYPAN C WITH ORTHOIMAGING/OMSIMAGING ACCESSORYEHD Extraoral with Timer X-Ray Unit
10 Nov 1997K973476KODAK DIGITAL SCIENCE-DENTAL IMAGE VIEWEREHD 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.