Guilin Kevin Peter Technology Co., Ltd.
FDA 510(k) & PMA Approved Devices — 4 products
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Total Devices4
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K261047 | Dental Diode Laser Device (Laser-Pen) | GEX | 2026-09-18 | View |
| 510(k) | K261695 | Flowable Restorative Material (KP-Flow LF, KP-Flow MF, KP-Flow HF) | EBF | 2026-08-31 | View |
| 510(k) | K261514 | Calcium Hydroxide Temporary Filling Material (KP-Cal) | KIF | 2026-08-25 | View |
| 510(k) | K261415 | Injectable Root Canal Sealer (KP-Root SP) | KIF | 2026-06-29 | View |
No matching devices.
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