Data / Medical devices / Italy / Axon SRL
Axon SRL: FDA-registered device maker in Pompei Napoli, Italy, 1 510(k) clearance
Axon SRL is registered with the FDA (registration 3030645016) in Pompei Napoli, Italy. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated August 30, 2023. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3030645016
- Address
- Via Lepanto 84, Pompei Napoli, Italy, 80045
- Owner or operator
- AXON SRL (10090398)
- Roles
- Manufacturer
- First device listed
- March 22, 2024
- Registered through
- 2026
- Brand names listed
- SPINERY RF Ablation System
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Electrosurgical, Cutting & Coagulation & Accessories | GEI | 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 |
|---|---|---|---|---|---|---|
| August 30, 2023 | K223303 | Spinery RF Ablation System | GEI | Substantially Equivalent | Axon Spine Medical System | accessdata.fda.gov |
Compare with other makers
Updated August 30, 2023. 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.