De Novo
DEN240076: Modius Lean
FDA De Novo · neurovalens limited · decided Oct 17, 2025
Key facts
| De Novo number | DEN240076 |
|---|---|
| Device name | Modius Lean |
| Applicant | neurovalens limited |
| Product code | SFW |
| Date received | Dec 18, 2024 |
| Decision date | Oct 17, 2025 |
| Decision | granted (DENG) |
| FDA classification | Class I |
| Review panel | Gastroenterology & Urology |
| FEI number | 3027997270 |
At a glance
- None Later 510(k)s citing this De Novo
- 1–9 UDI device identifiers (GUDID)
- None MAUDE adverse event reports
- None Recall events
- No Decision summary on file
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About De Novo classification requests
The De Novo pathway classifies novel low- to moderate-risk devices that have no legally marketed predicate; each granted request creates a new classification regulation and product code.
Source: U.S. Food and Drug Administration (FDA), De Novo database · Source date: