Manufacturer registered with FDA

AndersonBrecon Inc.

Rockford, IL, United States. Lists 2 dental device types with FDA across 1 registered establishment.

FDA owner/operator1417367Contract manufacturer
Device types listed
2
Brands and models
1
510(k) clearances
0as applicant
Markets registered in
21 registrations outside the US
Establishments
1United States

Registered in 2 markets

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

All markets
United States: 2 device types listedTaiwan: 1 registrations
RegisteredHome: United StatesOne marker per market
MarketRegulatorNamed asName on the registryRegistrationsIssuedRecords
United StatesFDAManufacturerAndersonBrecon Inc.2 device types—Below
TaiwanTFDAManufacturerANDERSON BRECON INC.12021–2021Pure 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 AndersonBrecon Inc. currently lists, by FDA device type, with the brand and model names on the listing.

Device typeCategoryRoleBrands and modelsListed since
Heat Source for Bleaching TeethEEG · Class 1Teeth whitening lightsMaker—2016
Polyvinyl Methylether Maleic Acid Calcium-Sodium Double Salt Denture AdhesiveKOO · Class 1Denture cleansers & adhesivesMaker
Fixodent
2012

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

Registered establishments

EstablishmentLocationWhat it does
ANDERSONBRECON INC.FDA reg. 1450819ROCKFORD, IL, United StatesContract manufacturer

Sources

FDA establishment registration & device listing (search FDA, owner/operator 1417367). 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.