Manufacturer registered with FDA
Stork Instrumente GmbH
EMMINGEN-LIPTINGEN 1, Germany. Lists 3 dental device types with FDA across 1 registered establishment.
- Device types listed
- 3
- Brands and models
- 0
- 510(k) clearances
- 0as applicant
- Markets registered in
- 419 registrations outside the US
- Establishments
- 1Germany
Registered in 4 markets
Where regulators' registries name Stork Instrumente GmbH 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 | Stork Instrumente GmbH | 3 device types | — | Below |
| Australia | TGA | Manufacturer | Stork Instrumente GmbH | 11 | 2004–2014 | Pure Global AI |
| South Korea | MFDS | Manufacturer | Stork Instrumente GMBHStork Instrumente GmbH | 6 | 2007–2009 | Pure Global AI |
| Taiwan | TFDA | Manufacturer | STORK INSTRUMENTE GMBH | 2 | 2005–2006 | 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 Stork Instrumente GmbH currently lists, by FDA device type, with the brand and model names on the listing.
| Device type | Category | Role | Brands and models | Listed since |
|---|---|---|---|---|
| Surgical Bone FileEMI · Class 1 | Dental hand instruments | Maker | — | 1998 |
| Dental Surgical CuretteEMK · Class 1 | Dental hand instruments | Maker | — | 1985 |
| Surgical Osteotome ChiselEMM · Class 1 | Dental hand instruments | Maker | — | 1985 |
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 |
|---|---|---|
| STORK INSTRUMENTE GMBHFDA reg. 8010547 | Emmingen-Liptingen Baden-Wurttemberg, Germany | Contract manufacturer |
Sources
FDA establishment registration & device listing (search FDA, owner/operator 8010547). 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.