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Sign in to claim this brandJeil Medical Corporation
South Korea·KR-MF-000008788
Last updated September 17, 2026
Part of Jeil Medical Corporation
What Jeil Medical Corporation makes
Jeil Medical Corporation manufactures orthopaedic hardware for internal bone fixation, including non-sliding bone screws, intramedullary nails, and non-bioabsorbable fixation plates for the femur, spine, and craniofacial regions. Their product line also includes polymeric spinal interbody fusion cages and specialized systems like the ARIX Hand System, ARIX Pectus Bar, and the FIX-L PEEK PLIF/T-PLIF for spinal and chest wall stabilization. Surgical instruments are provided as part of several orthopaedic systems. The company produces both sterile and non-sterile devices, with some products designed for specific anatomical applications such as hand and facial reconstruction.
The company’s devices are classified under FDA’s regulatory framework as Class I and Class II, with listings maintained in the FDA’s Unique Device Identifier (UDI) database. These classifications reflect varying levels of risk and regulatory oversight, depending on the device’s intended use and potential patient impact. The manufacturer operates from South Korea, adhering to domestic and international regulatory standards for medical devices.
Written from this company's registered devices by an AI model, and not verified by a human reviewer.
Information
- Country
- South Korea
- Address
- 702∙703∙704∙705∙706∙707∙804∙805∙807∙812∙815-ho, 55, Digital-ro 34-gil, Guro-gu, Seoul, 08378, Republic of Korea, Seoul, South Korea
- Website
- jeilmed.co.kr
- —
- —
- [email protected]
- Phone
- —
- PRRC Contact
- Sejin Ryu
- EUDAMED SRN
- KR-MF-000008788
- FDA FEI Number
- 3014937101
- DUNS Number
- 688811603
Catalogue (13359)
Page 4 of 268| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Summa Orthopaedics System Bone Screw | SO-35-SO-L30-T | FDA UDI | Class II | Active |
| Summa Orthopaedics System Bone Screw | SO-30-CS-020 | FDA UDI | Class II | Active |
| Summa Orthopaedics Femur Nail System | SO-PFN-0380-10R-30 | FDA UDI | Class II | Active |
| ARIX System Bone Screw | T141.031518 | FDA UDI | Class II | Active |
| Leforte System Bone Screw | 241.012320 | FDA UDI | Class II | Active |
| INLET System Bone Screw | IN27-AO-014-S | FDA UDI | Class II | Active |
| ARIX System Bone Screw | 20-HC-012 | FDA UDI | Class II | Active |
| Leforte System Bone Screw | 20L-MN-008 | FDA UDI | Class II | Active |
| ARIX Femur Nail System | 50I-SO-118-T | FDA UDI | Class II | Active |
| Leforte System Bone Plate | 16-SQ-004 | FDA UDI | Class II | Active |
| Arix | T141.012322.H | FDA UDI | Class II | Active |
| Arix | T141.012319 | FDA UDI | Class II | Active |
| ARIX Foot System Bone Plate | F23-LR-105-13 | FDA UDI | Class II | Active |
| Leforte System Bone Plate | 20-CH-004 | FDA UDI | Class II | Active |
| Dual Top Screw System / Dual Top Anchor System | 20-JD-008 | FDA UDI | Class II | Active |
| Prometheus Diaphysis System Bone Plate | PRO-10315 | FDA UDI | Class II | Active |
| ARIX System Bone Screw | 23-CS-030 | FDA UDI | Class II | Active |
| ARIX System Bone Screw | 35L-HF-014 | FDA UDI | Class II | Active |
| Dual Top Screw System / Dual Top Anchor System | 16-G2-012 | FDA UDI | Class II | Active |
| Xpine Spinal Fixation System | L69-P60A-8590 | FDA UDI | Class II | Active |
| ARIX System Bone Screw | 35L-SO-L32-TA | FDA UDI | Class II | Active |
| ARIX Femur Nail System | PFN-0280-13L-25 | FDA UDI | Class II | Active |
| Xpine Spinal Fixation System | L69-M60A-5050 | FDA UDI | Class II | Active |
| ARIX Femur Nail System | SPFC-005 | FDA UDI | Class II | Active |
| VERUM System Bone Screw | PH2020 | FDA UDI | Class II | Active |
| Summa Orthopaedics Femur Nail System | SO-S50I-SO-070-T | FDA UDI | Class II | Active |
| Leforte System Bone Plate | 242.51ST04 | FDA UDI | Class II | Active |
| Summa Orthopaedics System Surgical Instrument | SO-111-114 | FDA UDI | Class I | Active |
| INLET System Bone Screw | IN30-CH-026 | FDA UDI | Class II | Active |
| Prometheus Ankle System Bone Plate | PRO-10350 | FDA UDI | Class II | Active |
| Prometheus System Bone Screw | PRO-10040 | FDA UDI | Class II | Active |
| FIX-L PEEK PLIF and T-PLIF System | L68-081128-09 | FDA UDI | Class II | Active |
| FIX-L PEEK PLIF and T-PLIF System | L68-081022-14 | FDA UDI | Class II | Active |
| ARIX Femur Nail System | 50I-SO-060-T | FDA UDI | Class II | Active |
| INLET Clavicle System Bone Plate | IN35-SLCL-005-L | FDA UDI | Class II | Active |
| ARIX Pectus Bar System | PUP-350-TI | FDA UDI | Class II | Active |
| FIX-C PEEK Anterior Cervical Interbody System | C1-PCGS-09 | FDA UDI | Class II | Active |
| INLET System Bone Screw | IN30-CS-026L | FDA UDI | Class II | Active |
| INLET System Surgical Instrument | IN111-095-L | FDA UDI | Class I | Active |
| Xpine Spinal Fixation System | L69-RM60A-7085 | FDA UDI | Class II | Active |
| ARIX System Bone Screw | 30-CS-026 | FDA UDI | Class II | Active |
| FIX-L PEEK PLIF and T-PLIF System | L68-040930-14 | FDA UDI | Class II | Active |
| ARIX System Bone Screw | 28L-HF-022 | FDA UDI | Class II | Active |
| Drill bit | 112-12-201 | FDA UDI | Class I | Active |
| VERUM System Bone Screw | VF2316 | FDA UDI | Class II | Active |
| Summa Orthopaedics System Bone Screw | SO-30-CS-014 | FDA UDI | Class II | Active |
| Summa Orthopaedics Foot System Bone Plate | SO-35M-CLCC-206-R | FDA UDI | Class II | Active |
| VERUM System Surgical Instrument | CC0220 | FDA UDI | Class I | Active |
| ARIX Foot System Bone Plate | FW23-TL-705-08 | FDA UDI | Class II | Active |
| ARIX System Bone Screw | T141.032011.H | FDA UDI | Class II | Active |
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FDA Establishments (1)
Establishments registered with the FDA under this company group, matched by name.
- Jeil Medical Corporation Siheung-si Gyeonggi · KR FEI 3014937101