Data / Medical devices / United States / Nerbio Medical Software Platforms, Inc.
Nerbio Medical Software Platforms, Inc.: FDA-registered device maker in San Jose, CA, United States, 1 510(k) clearance
Nerbio Medical Software Platforms, Inc. is registered with the FDA (registration 3038371870) in San Jose, CA, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated December 5, 2024. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3038371870
- Address
- 1900 Camden Ave, San Jose, CA, United States, 95124
- Owner or operator
- Nerbio Medical Software Platforms, Inc. (10093243)
- Roles
- Specification developer
- First device listed
- April 17, 2025
- Registered through
- 2026
- Brand names listed
- iTOF
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Stimulator, Nerve, Peripheral, Electric | KOI | 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 |
|---|---|---|---|---|---|---|
| December 5, 2024 | K242525 | iTOF® | KOI | Substantially Equivalent | Nerbio Medical Software Platforms, Inc. | accessdata.fda.gov |
Compare with other makers
Updated December 5, 2024. 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.