Data / Medical devices / Argentina / Marzzan Lucas Jorge
Marzzan Lucas Jorge: FDA-registered device maker in Rosario Santa Fe, Argentina, 1 510(k) clearance
Marzzan Lucas Jorge is registered with the FDA (registration 3025488993) in Rosario Santa Fe, Argentina. It lists 3 device types. The FDA files 1 510(k) clearance under its listings, the newest dated January 31, 2025. Registered through 2026. FDA data exported November 3, 2026.
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- FDA registration number
- 3025488993
- Address
- Gdor. Crespo 1333, Rosario Santa Fe, Argentina, CP2000
- Owner or operator
- MARZZAN LUCAS JORGE (10092853)
- Roles
- Manufacturer
- First device listed
- February 26, 2025
- Registered through
- 2026
- Brand names listed
- Agilis Basic, Agilis Plus, Agilis Pro, Drop & Lift, E-Flex, Essential I, Essential II, Harmony and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Table, Mechanical | INW | 1 | Manufacturer | accessdata.fda.gov |
| Table, Physical Therapy, Multi Function | JFB | 2 | Manufacturer | accessdata.fda.gov |
| Table, Powered | INQ | 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 |
|---|---|---|---|---|---|---|
| January 31, 2025 | K241193 | AGILIS - Multi-function Physical Therapy Table (Model: Plus, Pro and Basic.) | JFB | Substantially Equivalent | Marzzan Lucas Jorge | accessdata.fda.gov |
Compare with other makers
- All makers of Table, Powered
- All makers of Table, Physical Therapy, Multi Function
- All makers of Table, Mechanical
Updated January 31, 2025. 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.