Data / Medical devices / Germany / NEXUS / CHILI GmbH
NEXUS / CHILI GmbH: FDA-registered device maker in DOSSENHEIM/HEIDELBERG Baden-Wurttemberg, Germany, 1 510(k) clearance
NEXUS / CHILI GmbH is registered with the FDA (registration 3006060685) in DOSSENHEIM/HEIDELBERG Baden-Wurttemberg, Germany. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated April 6, 2007. Registered through 2027. FDA data exported November 3, 2026.
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- FDA registration number
- 3006060685
- Address
- Friedrich-Ebert-Strasse 2, DOSSENHEIM/HEIDELBERG Baden-Wurttemberg, Germany, 69221
- Owner or operator
- NEXUS / CHILI GmbH (9091865)
- Roles
- Manufacturer
- First device listed
- June 8, 2007
- Registered through
- 2027
- Brand names listed
- CHILI PACS
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| System, Image Processing, Radiological | LLZ | 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 |
|---|---|---|---|---|---|---|
| April 6, 2007 | K070796 | CHILI PACS | LLZ | Substantially Equivalent | Chili GmbH | accessdata.fda.gov |
Compare with other makers
Updated April 6, 2007. 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.