Carbon, Inc.
FDA 510(k) & PMA Approved Devices — 1 products
Total Devices1
Categories1
Latest FDA decision2026-06-02
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K260569 | DB 4000 High Impact Denture Base | EBI | 2026-06-02 | View |
No matching devices.
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