Acculens, Inc.
FDA 510(k) & PMA Approved Devices — 1 products
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Total Devices1
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K230910 | NewVision SC (tisilfocon A) Scleral Lens; NewVision SC Daily Wear Ortho-K (tisilfocon A) Corneo-Scleral Lens | HQD | 2023-06-16 | View |
No matching devices.
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