Manufacturer registered with FDA

TIDI Products LLC

Neenah, WI, United States. Lists 6 dental device types with FDA across 1 registered establishment.

FDA owner/operator9921057Contract manufacturerManufacturerSpecification developer
Device types listed
6
Brands and models
0
510(k) clearances
0as applicant
Markets registered in
1287 registrations outside the US
Establishments
1United States

Registered in 12 markets

Where regulators' registries name TIDI Products LLC as the manufacturer or the registration holder of a device.

All markets
United States: 6 device types listedSaudi Arabia: 19 registrationsAustralia: 18 registrationsBrazil: 12 registrationsSouth Korea: 9 registrationsTaiwan: 9 registrationsColombia: 7 registrationsIsrael: 7 registrationsCanada: 2 registrationsEuropean Union: 2 registrationsCosta Rica: 1 registrationsSerbia: 1 registrations
RegisteredHome: United StatesOne marker per market
MarketRegulatorNamed asName on the registryRegistrationsIssuedRecords
United StatesFDAManufacturerTIDI Products LLC6 device types—Below
Saudi ArabiaSFDAManufacturerTIDI Products LLC19—Pure Global AI
AustraliaTGAManufacturerTIDI Products LLC182007–2025Pure Global AI
BrazilANVISAManufacturerTIDI PRODUCTS, LLCTIDI® Products, LLC122017–2025Pure Global AI
South KoreaMFDSManufacturerTIDI Products LLCTIDI Products, LLC · TIDI Products,LLC92005–2018Pure Global AI
TaiwanTFDAManufacturerTIDI PRODUCTS, LLCTIDI PRODUCTS LLC92012–2022Pure Global AI
ColombiaINVIMAManufacturerTIDI PRODUCTS, LLCTIDI PRODUCTS,LLC7—Pure Global AI
IsraelAMARManufacturerTIDI Products LLCTIDI Products, LLC · TIDI products LLC7—Pure Global AI
CanadaHealth CanadaRegistration holderTIDI PRODUCTS LLC.22011–2011Pure Global AI
European UnionEUDAMEDManufacturerTIDI Products, LLC.2—Pure Global AI
Costa RicaMinisterio de SaludManufacturerTIDI PRODUCTS LLC1—Pure Global AI
SerbiaALIMSManufacturerTIDI Products LLC12024–2024Pure 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 TIDI Products LLC currently lists, by FDA device type, with the brand and model names on the listing.

Device typeCategoryRoleBrands and modelsListed since
Operative Dental UnitEIA · Class 1Dental chairs & operative unitsMaker—2022
Air and/or Water Syringe UnitECB · Class 1Dental hand instrumentsMaker—2019
Roll CottonEFN · Class 1—Maker—2001
X-Ray Film HolderEGZ · Class 1—Maker—2008
Powered ToothbrushJEQ · Class 1ToothbrushesMaker—2021
Paper Saliva AbsorberKHR · Class 1—Maker—2002

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
TIDI PRODUCTS, LLCFDA reg. 2182318NEENAH, WI, United StatesContract manufacturer, Manufacturer, Specification developer

Sources

FDA establishment registration & device listing (search FDA, owner/operator 9921057). 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.