Data / Medical devices / Switzerland / Ares Trading SA
Ares Trading SA: FDA-registered device maker in Eysins Vaud, Switzerland, 1 510(k) clearance
Ares Trading SA is registered with the FDA (registration 3007115200) in Eysins Vaud, Switzerland. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated August 11, 1995. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3007115200
- FEI number
- 3002808103
- Address
- Route de Crassier 1, Eysins Vaud, Switzerland, 1262
- Owner or operator
- Ares Trading SA (10044883)
- Roles
- Specification developer
- First device listed
- December 3, 2019
- Registered through
- 2026
- Brand names listed
- Rebiject II
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Introducer, Syringe Needle | KZH | 2 | Specification developer | 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 |
|---|---|---|---|---|---|---|
| August 11, 1995 | K945660 | AUTOJECT 2 | KZH | Substantially Equivalent | Owen Mumford USA, Inc. | accessdata.fda.gov |
Compare with other makers
Updated August 11, 1995. 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.