Manufacturer registered with FDA
Anton Hipp GmbH
FRIDINGEN, Germany. Lists 1 dental device type with FDA across 1 registered establishment.
- Device types listed
- 1
- Brands and models
- 1
- 510(k) clearances
- 0as applicant
- Markets registered in
- 8347 registrations outside the US
- Establishments
- 1Germany
Registered in 8 markets
Where regulators' registries name Anton Hipp 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 | Anton Hipp GmbH | 1 device types | — | Below |
| Thailand | Thai FDA | Manufacturer | ANTON HIPP GMBH | 241 | — | Pure Global AI |
| South Korea | MFDS | Manufacturer | ANTON HIPP GMBHAnton Hipp GmbH · ANTON HIPP Gmbh · +1 | 39 | 2001–2025 | Pure Global AI |
| Saudi Arabia | SFDA | Manufacturer | Anton Hipp GmbH | 29 | — | Pure Global AI |
| Brazil | ANVISA | Manufacturer | ANTON HIPP GMBH | 20 | 2009–2026 | Pure Global AI |
| Australia | TGA | Manufacturer | Anton Hipp GmbH | 9 | 2004–2015 | Pure Global AI |
| Colombia | INVIMA | Manufacturer | ANTON HIPP GMBH | 5 | — | Pure Global AI |
| Taiwan | TFDA | Manufacturer | ANTON HIPP GMBH | 4 | 2006–2015 | 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 Anton Hipp 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 |
|---|---|---|---|---|
| Dental Surgical Tissue ScissorsEGN · Class 1 | Dental hand instruments | Maker | SCISSORS SURGICAL TISSUE DENTAL | 1994 |
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 |
|---|---|---|
| ANTON HIPP GMBHFDA reg. 8010528 | FRIDINGEN Baden-Wurttemberg, Germany | Manufacturer |
Sources
FDA establishment registration & device listing (search FDA, owner/operator 8010528). 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.