Not currently registered with FDA under this name

E.I. Dupont DE Nemours & Co., Inc.

Mchenry, IL, United States. Named as applicant on 1 dental 510(k) clearance between 1984 and 1984. No establishment is registered with FDA under this exact name today.

Device types listed
0
Brands and models
0
510(k) clearances
11984–1984
Markets registered in
21 registrations outside the US
Establishments
0—
1984: 119801990200020102020

510(k) clearances per year, 1980–2026

Registered in 2 markets

Where regulators' registries name E.I. Dupont DE Nemours & Co., Inc. as the manufacturer or the registration holder of a device.

All markets
United States: 1 clearancesTaiwan: 1 registrations
RegisteredHome: United StatesOne marker per market
MarketRegulatorNamed asName on the registryRegistrationsIssuedRecords
United StatesFDAApplicantE.I. Dupont DE Nemours & Co., Inc.1 clearances1984–1984Below
TaiwanTFDAManufacturerE.I. DU PONT DE NEMOURS & CO.11976–1976Pure 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 E.I. Dupont DE Nemours & Co., Inc. as the applicant.

Decided510(k)DeviceDevice type
13 Jan 1984K833701ACA THYROXINE ANALYTICAL TEST PACKLBH Cavity Varnish

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.