Agnes Medical Co., Ltd.
FDA 510(k) & PMA Approved Devices — 7 products
Total Devices7
Categories1
Latest Approval2025-09-03
| Type | Number | Device Name | Code | Date | |
|---|---|---|---|---|---|
| 510(k) | K250217 | AGNES Ultra | GEI | 2025-09-03 | View |
| 510(k) | K243713 | Single Use RF Surgical Electrode (Needle Type) (AN-B, AN-C, AN-E, AN-I, AN-S, AN-W3A, AN-F3A, AN-IL, AN-SL, AN-W3B, AN-F1A, AN-F3B, AN-B3A) | GEI | 2025-08-19 | View |
| 510(k) | K242469 | RFMagik Lite | GEI | 2025-04-25 | View |
| 510(k) | K230837 | PlazMagik | GEI | 2024-02-29 | View |
| 510(k) | K223805 | Agnes | GEI | 2023-05-04 | View |
| 510(k) | K203013 | AGNES | GEI | 2022-07-14 | View |
| 510(k) | K192728 | Agnes | GEI | 2019-10-24 | View |
No matching devices.