Glaukos Corporation
Glaukos Corporation appears in FDA public data with 0 recalls, 1 510(k) clearance, 7 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on August 2, 2022.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 1
- Inspections
- 7
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K220032 | iStent infinite Trabecular Micro-Bypass System, Model iS3 | August 2, 2022 |