Not currently registered with FDA under this name
Uresil Corp.
Skokie, IL, United States. Named as applicant on 1 dental 510(k) clearance between 1990 and 1990. No establishment is registered with FDA under this exact name today.
- Device types listed
- 0
- Brands and models
- 0
- 510(k) clearances
- 11990–1990
- Markets registered in
- 15126 registrations outside the US
- Establishments
- 0—
510(k) clearances per year, 1990–2026
Registered in 15 markets
Where regulators' registries name Uresil Corp. as the manufacturer or the registration holder of a device.
RegisteredHome: United StatesOne marker per market
| Market | Regulator | Named as | Name on the registry | Registrations | Issued | Records |
|---|---|---|---|---|---|---|
| United States | FDA | Applicant | Uresil Corp. | 1 clearances | 1990–1990 | Below |
| Canada | Health Canada | Registration holder | URESIL | 22 | 2004–2024 | Pure Global AI |
| United Kingdom | MHRA | Manufacturer | UreSil, LLC | 22 | — | Pure Global AI |
| Saudi Arabia | SFDA | Manufacturer | UreSil, LLC | 20 | — | Pure Global AI |
| Costa Rica | Ministerio de Salud | Manufacturer | Uresil, LLC | 9 | — | Pure Global AI |
| Serbia | ALIMS | Manufacturer | Uresil LLC | 8 | 2024–2024 | Pure Global AI |
| South Korea | MFDS | Manufacturer | UreSil L.L.C.UreSil, LLC. · Uresil · +2 | 8 | 2006–2011 | Pure Global AI |
| Australia | TGA | Manufacturer | Uresil LLC | 7 | 2025–2025 | Pure Global AI |
| Colombia | INVIMA | Manufacturer | URESIL, LLC | 7 | — | Pure Global AI |
| Taiwan | TFDA | Manufacturer | URESIL, LLCURESIL CORPORATION | 5 | 1992–2017 | Pure Global AI |
| Brazil | ANVISA | Manufacturer | URESIL LLC | 4 | 2006–2015 | Pure Global AI |
| European Union | EUDAMED | Registration holder | UreSil, LLC | 4 | — | Pure Global AI |
| Israel | AMAR | Manufacturer | Uresil LLCURESIL | 4 | — | Pure Global AI |
| China | NMPA | Registration holder | 美国优士有限公司UreSil, LLC美国优士有限公司UreSil,LLC | 3 | — | Pure Global AI |
| Peru | DIGEMID | Manufacturer | URESIL LLC | 3 | 2013–2023 | 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
Sources
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 of the most recent filing, which can be a US agent.