Manufacturer registered with FDA

Spectrum Plastics Group

Minneapolis, MN, United States. Lists 1 dental device type with FDA across 1 registered establishment.

FDA owner/operator9050399Contract manufacturer
Device types listed
1
Brands and models
0
510(k) clearances
0as applicant
Markets registered in
22 registrations outside the US
Establishments
1United States

Registered in 2 markets

Where regulators' registries name Spectrum Plastics Group as the manufacturer or the registration holder of a device.

All markets
United States: 1 device types listedTaiwan: 2 registrations
RegisteredHome: United StatesOne marker per market
MarketRegulatorNamed asName on the registryRegistrationsIssuedRecords
United StatesFDAManufacturerSpectrum Plastics Group1 device types—Below
TaiwanTFDAManufacturerSPECTRUM PLASTICS GROUP22017–2021Pure 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 Spectrum Plastics Group currently lists, by FDA device type, with the brand and model names on the listing.

Device typeCategoryRoleBrands and modelsListed since
Polishing Agent WheelEJQ · Class 1Polishing & prophylaxisMaker—2016

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
Spectrum Plastics GroupFDA reg. 2183967Saint Louis Park, MN, United StatesContract manufacturer

Sources

FDA establishment registration & device listing (search FDA, owner/operator 9050399). 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.