Jeil Medical Corporation
Jeil Medical Corporation holds FDA 510(k) medical device clearances, first cleared 2002, most recent 2026.
Top product codes for Jeil Medical Corporation
Recent clearances by Jeil Medical Corporation
- K252246 — Leforte MMF System
- K252826 — ARIX Femur Nail System
- K251431 — FIX-C PEEK ACIF SA System
- K243973 — FIX-L PEEK PLIF and T-PLIF System
- K242751 — ARIX Pectus Bar System
- K242247 — ARIX Femur Nail System
- K243915 — FIX-C 3D Ti ACIF System
- K243004 — Xpine Spinal Fixation System
- K231251 — FlexWing Anterior Cervical Plate System
- K233912 — ARIX Cannulated Screw System
- K231887 — ARIX Ankle Distal Tibia System
- K231441 — ARIX Ankle System
- K230938 — ARIX Humerus System
- K221412 — ARIX Rib System
- K221920 — ARIX Small Fragment System
- K212266 — FIX-C PEEK Anterior Cervical Interbody System
- K202912 — ARIX Ankle Distal Tibia System
- K201656 — ARIX Elbow System
- K193616 — ARIX Ankle System
- K192417 — ARIX Cannulated Screw System
- K191972 — ARIX Wrist System
- K181806 — ARIX Sternal System
- K180972 — ARIX Clavicle System
- K172008 — ARIX Humerus System
- K170705 — ARIX Wrist System
- K170368 — Sterile NS System
- K170979 — ARIX Ankle Fibula Hook Plate System
- K170780 — ARIX Foot System (2.3/2.8)
- K170313 — ARIX Ankle Distal Tibia System
- K171285 — ARIX Diaphysis System
- K161335 — Dual Top Screw System
- K163308 — SMARTO
- K161746 — ARIX Hand System
- K161864 — ARIX Foot System
- K151468 — ARIX Wrist System
- K152158 — ARIX Ankle System
- K150965 — LeForte System II
- K143730 — GBR System
- K130447 — SPEEDY FLAP SYSTEM
- K141452 — LEFORTE NEURO SYSTEM BONE PLATE AND SCREW
- K132876 — ARIX HAND LOCKING SYSTEM
- K131566 — ARIX HAND SYSTEM
- K131311 — ARIX FOOT SYSTEM
- K112812 — LEFORTE NEURO SYSTEM BONE PLATE
- K101902 — J TAC MODEL JT-MD-035, JT-MD-040, JT-MD-045, JT-CL-030
- K103778 — LEFORTE NEURO SYSTEM BONE PLATE
- K101563 — SMARTO
- K091686 — LEFORTE NEUROSYSTEM BONE SCREW
- K091679 — LEFORTE SYSTEM BONE PLATE
- K050669 — JEIL BONE FIXATION SYSTEM
- K033767 — DUAL TOP ANCHOR SYSTEM SCREWS
- K023365 — LEFORTE SYSTEM BONE SCREW
- K023360 — LEFORTE SYSTEM BONE PLATE
Data sourced from openFDA. This site is unofficial and independent of the FDA.