PMA
P240020: TOUCH® CMC 1 Prosthesis
FDA PMA · Prosthesis, finger, semi-constrained, metal/polymer · Keri Medical SA
Key facts
| PMA number | P240020 |
|---|---|
| Trade name | TOUCH® CMC 1 Prosthesis |
| Generic name | Prosthesis, finger, semi-constrained, metal/polymer |
| Applicant | Keri Medical SA |
| Owner/operator | Keri Medical |
| Product code | SFA |
| Approval date | Jul 10, 2025 |
| Docket number | 25M-2274 |
| Notice date | Jul 11, 2025 |
| Establishment registration | 3024706750 |
| FEI number | 3024706750 |
At a glance
- 1–9 Supplements
- Jun 24, 2026 Latest supplement decision
- No Withdrawn
- Yes Summary of safety and effectiveness on file
- 10–99 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: