PMA supplement
P230002 S002: Minitouch 3.8 Era System (Minitouch System)
FDA PMA supplement · Normal 180 Day Track · Microcube, LLC
Key facts
| Original PMA | P230002 |
|---|---|
| Supplement number | S002 |
| Supplement type | Normal 180 Day Track |
| Reason for the supplement | Change Design/Components/Specifications/Material |
| Trade name | Minitouch 3.8 Era System (Minitouch System) |
| Generic name | Device, thermal ablation, endometrial |
| Applicant | Microcube, LLC |
| Product code | MNB |
| Received date | Dec 5, 2025 |
| Decision date | Jul 13, 2026 |
At a glance
- No Expedited review granted
- No Approval order on file
- No Summary of safety and effectiveness on file
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About PMA supplements
A PMA supplement asks FDA to approve a change to a device that already holds a premarket approval: a new indication, a design or labeling change, a manufacturing site or process change.
Source: U.S. Food and Drug Administration (FDA), Premarket Approval (PMA) database · Source date: