PMA
P250016: Belotero® Intense (+) Lidocaine
FDA PMA · Implant, dermal, for aesthetic use · Merz North America, Inc.
Key facts
| PMA number | P250016 |
|---|---|
| Trade name | Belotero® Intense (+) Lidocaine |
| Generic name | Implant, dermal, for aesthetic use |
| Applicant | Merz North America, Inc. |
| Product code | LMH |
| Approval date | Jul 9, 2026 |
| Docket number | 26M-7708 |
| Notice date | Jul 9, 2026 |
At a glance
- 1–9 Supplements
- Aug 31, 2026 Latest supplement decision
- No Withdrawn
- Yes Summary of safety and effectiveness on file
- None UDI device identifiers (GUDID)
- None MAUDE adverse event reports
- None Recall events
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About PMA approvals
Premarket approval (PMA) is the FDA's most stringent review pathway, required for most Class III devices that support or sustain life or present a potentially unreasonable risk.
Source: U.S. Food and Drug Administration (FDA), Premarket Approval (PMA) database · Source date: