De Novo
DEN250026: Avulux
FDA De Novo · matap ii, llc · decided Aug 21, 2026
Key facts
| De Novo number | DEN250026 |
|---|---|
| Device name | Avulux |
| Applicant | matap ii, llc |
| Product code | QEO |
| Date received | Jun 23, 2025 |
| Decision date | Aug 21, 2026 |
| Decision | granted (DENG) |
| FDA classification | Class I |
| Review panel | Neurology |
| FEI number | 3014942931 |
At a glance
- None Later 510(k)s citing this De Novo
- None 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: