Data / Medical devices / Germany / Ritter Implants GmbH & Co. KG
Ritter Implants GmbH & Co. KG: FDA-registered device maker in Biberach Baden-Wurttemberg, Germany, 3 510(k) clearances
Ritter Implants GmbH & Co. KG is registered with the FDA (registration 3009528809) in Biberach Baden-Wurttemberg, Germany. It lists 4 device types. The FDA files 3 510(k) clearances under its listings, the newest dated January 24, 2019. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3009528809
- Address
- Freiburger Str. 45, Biberach Baden-Wurttemberg, Germany, 88400
- Owner or operator
- Ritter Implants GmbH and Co. KG (10047159)
- Roles
- Manufacturer
- First device listed
- July 9, 2014
- Registered through
- 2026
- Brand names listed
- CD-2.5, CD-2.8, CD-3, CD-3.3, CD-3.75, CD-3.75-4.2, CD-4.2, CD-5 and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Abutment, Implant, Dental, Endosseous | NHA | 2 | Manufacturer | accessdata.fda.gov |
| Accessories, Implant, Dental, Endosseous | NDP | 1 | Manufacturer | accessdata.fda.gov |
| Drill, Dental, Intraoral | DZA | 1 | Manufacturer | accessdata.fda.gov |
| Implant, Endosseous, Root-Form | DZE | 2 | Manufacturer | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| January 24, 2019 | K180183 | Ritter Dental Implant System | DZE | Substantially Equivalent | Ritter Implants GmbH & Co. KG | accessdata.fda.gov |
| December 14, 2016 | K160475 | Ritter Dental Implant System | DZE | Substantially Equivalent | Ritter Implants GmbH & Co. KG | accessdata.fda.gov |
| May 9, 2014 | K131557 | RITTER IMPLANT SYSTEM | DZE | Substantially Equivalent | Ritter Implants GmbH CO KG | accessdata.fda.gov |
Compare with other makers
- All makers of Drill, Dental, Intraoral
- All makers of Abutment, Implant, Dental, Endosseous
- All makers of Implant, Endosseous, Root-Form
- All makers of Accessories, Implant, Dental, Endosseous
Updated January 24, 2019. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.