Manufacturer registered with FDA
G. Hipp & Sohn GmbH
NEUHAUSEN OB ECK, Germany. Lists 2 dental device types with FDA across 1 registered establishment.
- Device types listed
- 2
- Brands and models
- 0
- 510(k) clearances
- 0as applicant
- Markets registered in
- 21 registrations outside the US
- Establishments
- 1Germany
Registered in 2 markets
Where regulators' registries name G. Hipp & Sohn 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 | G. Hipp & Sohn GmbH | 2 device types | — | Below |
| South Korea | MFDS | Manufacturer | G. Hipp & Sohn GmbH | 1 | 2002–2002 | 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 G. Hipp & Sohn 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 |
|---|---|---|---|---|
| All Types RetractorEIG · Class 1 | Dental hand instruments | Maker | — | 2021 |
| Surgical Osteotome ChiselEMM · Class 1 | Dental hand instruments | Maker | — | 2000 |
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 |
|---|---|---|
| G. HIPP & SOHN GMBHFDA reg. 8010252 | NEUHAUSEN Baden-Wurttemberg, Germany | Contract manufacturer |
Sources
FDA establishment registration & device listing (search FDA, owner/operator 8010253). 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.