Manufacturer registered with FDA
Goldman Products, Inc.
Wauconda, IL, United States. Lists 18 dental device types with FDA across 1 registered establishment.
- Device types listed
- 18
- Brands and models
- 36
- 510(k) clearances
- 0as applicant
- Markets registered in
- 331 registrations outside the US
- Establishments
- 1United States
Registered in 3 markets
Where regulators' registries name Goldman Products, Inc. as the manufacturer or the registration holder of a device.
| Market | Regulator | Named as | Name on the registry | Registrations | Issued | Records |
|---|---|---|---|---|---|---|
| United States | FDA | Manufacturer | Goldman Products, Inc. | 18 device types | — | Below |
| South Korea | MFDS | Manufacturer | Goldman Products, Inc. | 30 | 2010–2012 | Pure Global AI |
| Israel | AMAR | Manufacturer | GOLDMAN PRODUCTS INC | 1 | — | Pure 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 Goldman Products, Inc. currently lists, by FDA device type, with the brand and model names on the listing.
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
| Establishment | Location | What it does |
|---|---|---|
| GOLDMAN PRODUCTS, INC.FDA reg. 1419982 | WAUCONDA, IL, United States | Contract manufacturer, Manufacturer, Remanufacturer |
Sources
FDA establishment registration & device listing (search FDA, owner/operator 1419982). 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.