De Novo
DEN160029: SkinPen Precision System
FDA De Novo · bellus medical, llc. · decided Mar 1, 2018
Key facts
| De Novo number | DEN160029 |
|---|---|
| Device name | SkinPen Precision System |
| Applicant | bellus medical, llc. |
| Product code | QAI |
| Date received | Jul 5, 2016 |
| Decision date | Mar 1, 2018 |
| Decision | granted (DENG) |
| FDA classification | Class II |
| Review panel | General & Plastic Surgery |
| FEI number | 3010392991 |
At a glance
- 10–99 Later 510(k)s citing this De Novo
- 1–9 UDI device identifiers (GUDID)
- 1–9 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: