Jeil Medical Corporation
FDA 510(k) & PMA Approved Devices — 35 products
Total Devices35
Categories12
Latest FDA decision2026-04-02
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K191972 | ARIX Wrist System | HRS | 2019-11-12 | View |
| 510(k) | K181806 | ARIX Sternal System | HRS | 2018-11-20 | View |
| 510(k) | K180972 | ARIX Clavicle System | HRS | 2018-10-03 | View |
| 510(k) | K172008 | ARIX Humerus System | HRS | 2017-12-01 | View |
| 510(k) | K170705 | ARIX Wrist System | HRS | 2017-09-21 | View |
| 510(k) | K170368 | Sterile NS System | GWO | 2017-09-11 | View |
| 510(k) | K170979 | ARIX Ankle Fibula Hook Plate System | HRS | 2017-08-17 | View |
| 510(k) | K170780 | ARIX Foot System (2.3/2.8) | HRS | 2017-08-14 | View |
| 510(k) | K170313 | ARIX Ankle Distal Tibia System | HRS | 2017-07-27 | View |
| 510(k) | K171285 | ARIX Diaphysis System | HRS | 2017-07-24 | View |
| 510(k) | K161335 | Dual Top Screw System | OAT | 2017-02-23 | View |
| 510(k) | K163308 | SMARTO | KIJ | 2016-12-27 | View |
| 510(k) | K161746 | ARIX Hand System | HRS | 2016-09-21 | View |
| 510(k) | K161864 | ARIX Foot System | HRS | 2016-08-02 | View |
| 510(k) | K151468 | ARIX Wrist System | HRS | 2016-01-14 | View |
No matching devices.
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