PMA supplement
P170043 S023: Glaukos® iStent inject® W Trabecular Micro-Bypass System, Glaukos® iStent inject® W Trabecular Micro-Bypass System with
FDA PMA supplement · 30-Day Notice · Glaukos Corporation
Key facts
| Original PMA | P170043 |
|---|---|
| Supplement number | S023 |
| Supplement type | 30-Day Notice |
| Reason for the supplement | Process Change - Manufacturer/Sterilizer/Packager/Supplier |
| Trade name | Glaukos® iStent inject® W Trabecular Micro-Bypass System, Glaukos® iStent inject® W Trabecular Micro-Bypass System with |
| Generic name | Intraocular pressure lowering implant |
| Applicant | Glaukos Corporation |
| Product code | OGO |
| Received date | Sep 1, 2026 |
| Decision date | Oct 1, 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: