Data / Medical devices / Germany / Ritter Concept GMBH
Ritter Concept GMBH: FDA-registered device maker in Biberach Baden-Wurttemberg, Germany, 1 510(k) clearance
Ritter Concept GMBH is registered with the FDA (registration 3008813313) in Biberach Baden-Wurttemberg, Germany. It lists 3 device types. The FDA files 1 510(k) clearance under its listings, the newest dated December 9, 2016. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3008813313
- Address
- Freiburger Str. 45, Biberach Baden-Wurttemberg, Germany, 88400
- Owner or operator
- Ritter Concept GmbH (10039718)
- Roles
- Manufacturer
- First device listed
- February 6, 2012
- Registered through
- 2026
- Brand names listed
- Contact Lite, Contact Lite Comfort, Contact World, Hanging, Ritter, Swinging, Ultimate Comfort, Ultimate Comfort Smart and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Unit, Operative Dental | EIA | 1 | Manufacturer | accessdata.fda.gov |
| Unit, Operative Dental, Accessories | NRD | 1 | Manufacturer | accessdata.fda.gov |
| Unit, Suction Operatory | EBR | 1 | 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 |
|---|---|---|---|---|---|---|
| December 9, 2016 | K161734 | Vanguard Dental Unit | EIA | Substantially Equivalent | Ritter Concept GmbH | accessdata.fda.gov |
Compare with other makers
- All makers of Unit, Operative Dental, Accessories
- All makers of Unit, Operative Dental
- All makers of Unit, Suction Operatory
Updated December 9, 2016. 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.