Manufacturer registered with FDA
Schott AG
Mainz, Germany. Lists 1 dental device type with FDA across 1 registered establishment.
- Device types listed
- 1
- Brands and models
- 2
- 510(k) clearances
- 0as applicant
- Markets registered in
- 32 registrations outside the US
- Establishments
- 1Germany
Registered in 3 markets
Where regulators' registries name Schott AG 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 | Schott AG | 1 device types | — | Below |
| South Korea | MFDS | Manufacturer | Schott AG | 1 | 2011–2011 | Pure Global AI |
| Taiwan | TFDA | Manufacturer | SCHOTT AG | 1 | 2015–2015 | 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 Schott AG currently lists, by FDA device type, with the brand and model names on the listing.
| Device type | Category | Role | Brands and models | Listed since |
|---|---|---|---|---|
| Ultraviolet Activator for PolymerizationEBZ · Class 2 | Curing lights | Maker | Fiber Optic RodLight, Fiberoptic, Dental | 2023 |
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 |
|---|---|---|
| SCHOTT AGFDA reg. 3006984721 | Mainz Rhineland-Palatinate, Germany | Contract manufacturer |
Sources
FDA establishment registration & device listing (search FDA, owner/operator 10025267). 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.