Not currently registered with FDA under this name

Remington Medical, Inc.

Atlanta, GA, United States. Named as applicant on 1 dental 510(k) clearance between 1995 and 1995. No establishment is registered with FDA under this exact name today.

Device types listed
0
Brands and models
0
510(k) clearances
11995–1995
Markets registered in
943 registrations outside the US
Establishments
0—
1995: 11990200020102020

510(k) clearances per year, 1990–2026

Registered in 9 markets

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

All markets
United States: 1 clearancesCanada: 27 registrationsBrazil: 5 registrationsUnited Kingdom: 4 registrationsSouth Korea: 3 registrationsAustralia: 1 registrationsEuropean Union: 1 registrationsSaudi Arabia: 1 registrationsTaiwan: 1 registrations
RegisteredHome: United StatesOne marker per market
MarketRegulatorNamed asName on the registryRegistrationsIssuedRecords
United StatesFDAApplicantRemington Medical, Inc.1 clearances1995–1995Below
CanadaHealth CanadaRegistration holderREMINGTON MEDICAL, INC.272004–2018Pure Global AI
BrazilANVISAManufacturerREMINGTON MEDICAL, INC.52011–2014Pure Global AI
United KingdomMHRAManufacturerREMINGTON MEDICAL INC4—Pure Global AI
South KoreaMFDSManufacturerRemington Medical, Inc.Remington Medical, S.A.32019–2025Pure Global AI
AustraliaTGAManufacturerRemington Medical Inc12018–2018Pure Global AI
European UnionEUDAMEDManufacturerRemington Medical, Inc.1—Pure Global AI
Saudi ArabiaSFDAManufacturerRemington Medical, Inc.1—Pure Global AI
TaiwanTFDAManufacturerRemington Medical, Inc.12022–2022Pure 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 Remington Medical, Inc. as the applicant.

Decided510(k)DeviceDevice type
2 Oct 1995K953812GAUZE SPONGEKHR Paper Saliva Absorber

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.