PMA supplement
P030028 S013: ARTISAN Myopia Models 204US1W and 206US1W
FDA PMA supplement · 30-Day Notice · Ophtec BV
Key facts
| Original PMA | P030028 |
|---|---|
| Supplement number | S013 |
| Supplement type | 30-Day Notice |
| Reason for the supplement | Process Change - Manufacturer/Sterilizer/Packager/Supplier |
| Trade name | ARTISAN Myopia Models 204US1W and 206US1W |
| Generic name | Lens, intraocular, phakic |
| Applicant | Ophtec BV |
| Product code | MTA |
| Received date | Nov 12, 2025 |
| Decision date | Apr 24, 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: