Not currently registered with FDA under this name

Ritter Co.

Mchenry, IL, United States. Named as applicant on 6 dental 510(k) clearances between 1976 and 1983. No establishment is registered with FDA under this exact name today.

Device types listed
0
Brands and models
0
510(k) clearances
61976–1983
Markets registered in
32 registrations outside the US
Establishments
0—
1976: 21978: 11980: 11982: 11983: 119801990200020102020

510(k) clearances per year, 1976–2026

Registered in 3 markets

Where regulators' registries name Ritter Co. as the manufacturer or the registration holder of a device.

All markets
United States: 6 clearancesEuropean Union: 1 registrationsUnited Kingdom: 1 registrations
RegisteredHome: United StatesOne marker per market
MarketRegulatorNamed asName on the registryRegistrationsIssuedRecords
United StatesFDAApplicantRitter Co.6 clearances1976–1983Below
European UnionEUDAMEDManufacturerRitter GmbH1—Pure Global AI
United KingdomMHRAManufacturerRitter GmbH1—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 Ritter Co. as the applicant.

Decided510(k)DeviceDevice type
12 Aug 1983K831976POWER OPTICEAY Dental Fiber Optic Light
22 Nov 1982K823180SA-21 DENTAL UNITEIA Operative Dental Unit
29 Jan 1980K800084RITTER MODEL J DENTAL CHAIRKLC Dental Chair with Operative Unit
3 Jan 1978K772300DENTAL CHAIR, VANGUARDKLC Dental Chair with Operative Unit
19 Nov 1976K760929ACCUTORQ IIEFB Dental Air-Powered Handpiece
5 Oct 1976K760707RITTER STARLIGHT DENTAL OPERATING LIGHTEAZ Dental Operating Light

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.