Jeil Medical Corporation
FDA 510(k) medical device clearances.
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.