Data / Medical devices / Belgium / Euromi S.A.
Euromi S.A.: FDA-registered device maker in Andrimont Liege, Belgium, 2 510(k) clearances
Euromi S.A. is registered with the FDA (registration 3007697975) in Andrimont Liege, Belgium. It lists 2 device types. The FDA files 2 510(k) clearances under its listings, the newest dated December 16, 2010. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3007697975
- Address
- Rue des Nouvelles Technologies, 11 ZI des Plenesses, Andrimont Liege, Belgium, 4821
- Owner or operator
- Euromi S.A. (10056094)
- Roles
- Manufacturer
- First device listed
- August 27, 2018
- Registered through
- 2026
- Brand names listed
- EVA SP6, LIPOMATIC / EVAMATIC, NLF SYSTEM Kit 2 (EUROMI)
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Lipoaspirate Washing System For Aesthetic Body Contouring | QKL | 2 | Manufacturer | accessdata.fda.gov |
| System, Suction, Lipoplasty For Removal | QPB | 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 |
|---|---|---|---|---|---|---|
| December 16, 2010 | K101413 | EUROMI EVA SP6 | QPB | Substantially Equivalent | Euromi S.A | accessdata.fda.gov |
| June 29, 2001 | K010311 | LIPOMATIC; LIPOMATIC LIPOSUCTION DEVICE | QPB | Substantially Equivalent | Euromi S.A | accessdata.fda.gov |
Compare with other makers
- All makers of System, Suction, Lipoplasty For Removal
- All makers of Lipoaspirate Washing System For Aesthetic Body Contouring
Updated December 16, 2010. 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.