Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

Jeil Medical Corporation

FDA 510(k) & PMA Approved Devices — 35 products

Total Devices35
Categories12
Latest FDA decision2026-04-02
TypeNumberDevice NameCodeDateActions
510(k) K191972 ARIX Wrist SystemHRS2019-11-12 View
510(k) K181806 ARIX Sternal SystemHRS2018-11-20 View
510(k) K180972 ARIX Clavicle SystemHRS2018-10-03 View
510(k) K172008 ARIX Humerus SystemHRS2017-12-01 View
510(k) K170705 ARIX Wrist SystemHRS2017-09-21 View
510(k) K170368 Sterile NS SystemGWO2017-09-11 View
510(k) K170979 ARIX Ankle Fibula Hook Plate SystemHRS2017-08-17 View
510(k) K170780 ARIX Foot System (2.3/2.8)HRS2017-08-14 View
510(k) K170313 ARIX Ankle Distal Tibia SystemHRS2017-07-27 View
510(k) K171285 ARIX Diaphysis SystemHRS2017-07-24 View
510(k) K161335 Dual Top Screw SystemOAT2017-02-23 View
510(k) K163308 SMARTOKIJ2016-12-27 View
510(k) K161746 ARIX Hand SystemHRS2016-09-21 View
510(k) K161864 ARIX Foot SystemHRS2016-08-02 View
510(k) K151468 ARIX Wrist SystemHRS2016-01-14 View

Page 2 of 2