Manufacturer registered with FDA

Aurident, Inc.

Fullerton, CA, United States. Lists 3 dental device types with FDA across 1 registered establishment, and holds 1 510(k) clearance as applicant.

FDA owner/operator2023817Contract manufacturerManufacturerRepacker / relabeler
Device types listed
3
Brands and models
3
510(k) clearances
12004–2004
Markets registered in
212 registrations outside the US
Establishments
1United States
2004: 1200020102020

510(k) clearances per year, 2000–2026

Registered in 2 markets

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

All markets
United States: 3 device types listedCanada: 12 registrations
RegisteredHome: United StatesOne marker per market
MarketRegulatorNamed asName on the registryRegistrationsIssuedRecords
United StatesFDAManufacturerAurident, Inc.1 clearances2004–2004Below
CanadaHealth CanadaRegistration holderAURIDENT, INC.122006–2006Pure 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

Devices listed with FDA

What Aurident, Inc. currently lists, by FDA device type, with the brand and model names on the listing.

Device typeCategoryRoleBrands and modelsListed since
Porcelain PowderEIH · Class 2Dental ceramics & zirconiaLister
Delta Zirconia
2007
Alloy Other Noble MetalEJS · Class 2Dental alloysMaker
Aurident Alloys
2003
Gold-Based Noble Metal AlloyEJT · Class 2Dental alloysMaker
Aurident Alloys
2003

Source: FDA establishment registration & device listing, 510(k) and product classification files · FDA data as of 2 Nov 2026 · snapshot 12 Nov 2026

510(k) clearances

Clearances on which FDA names Aurident, Inc. as the applicant.

Decided510(k)DeviceDevice type
17 Dec 2004K042638RADIANCE PORCELAINEIH Porcelain Powder

Registered establishments

EstablishmentLocationWhat it does
AURIDENT, INC.FDA reg. 2023817FULLERTON, CA, United StatesContract manufacturer, Manufacturer, Repacker / relabeler

Sources

FDA establishment registration & device listing (search FDA, owner/operator 2023817). 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.