De Novo
DEN260007: SmartRead(TM) Medical Device Identifier (4100)
FDA De Novo · bridgesource medical corporation · decided Sep 29, 2026
Key facts
| De Novo number | DEN260007 |
|---|---|
| Device name | SmartRead(TM) Medical Device Identifier (4100) |
| Applicant | bridgesource medical corporation |
| Product code | SJJ |
| Date received | Mar 24, 2026 |
| Decision date | Sep 29, 2026 |
| Decision | granted (DENG) |
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: