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Sign in to claim this brandCorentec Co., Ltd
US
Last updated May 24, 2026
What Corentec Co., Ltd makes
Corentec Co., Ltd manufactures spinal fixation hardware, including non-bioabsorbable bone screws, polymeric spinal fusion cages, and internal fixation rods for interbody and lateral applications. Their portfolio also includes knee replacement components such as reusable trial prostheses for the tibia and femur, tibial inserts, and modular knee systems for surgical planning. These devices are designed for orthopedic procedures, including spinal stabilization and total knee arthroplasty.
The company’s devices are classified under FDA categories, with most falling into Class I or Class II, and are listed in the FDA’s Unique Device Identifier (UDI) database. The manufacturer operates from the United States, adhering to regulatory requirements for medical devices in that jurisdiction.
Written from this company's registered devices by an AI model, and not verified by a human reviewer.
Information
- Country
- US
- Address
- —
- Website
- corentec.com
- —
- —
- [email protected]
- Phone
- +82269374902
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- —
- DUNS Number
- 688739895
Catalogue (9707)
Page 36 of 195| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| LOSPA IS Spinal System | SI.C30.0911 | FDA UDI | Class II | Active |
| BENCOX Hip System | HA.01D.0060 | FDA UDI | Class II | Active |
| LOSPA Modular Knee System | K2.C12.0020 | FDA UDI | Class II | Active |
| LOSPA IS Spinal System | SC.V02.4512 | FDA UDI | Class II | Active |
| EXULT Knee Replacement System | KA.CFT.L013-SUS | FDA UDI | Class II | Active |
| LOSPA IS Spinal Fixation System | SA.227.8085 | FDA UDI | Class II | Active |
| LOSPA IS Spinal Fixation System | SA.223.6030 | FDA UDI | Class II | Active |
| LOSPA Knee System | KD.STT.LC10 | FDA UDI | Class II | Active |
| LOSPA IS Spinal System | SC.H17.2411 | FDA UDI | Class II | Active |
| LOSPA IS Spinal Fixation System | SA.228.7095 | FDA UDI | Class II | Active |
| LOSPA IS Spinal Fixation System | SA.221.8055 | FDA UDI | Class II | Active |
| LOSPA IS Spinal System | SM.C53.0510 | FDA UDI | Class II | Active |
| LOSPA Knee System | 01.62.26I | FDA UDI | Class II | Active |
| LOSPA IS Spinal System | 01.22.611 | FDA UDI | Class II | Active |
| LOSPA Total Knee System | 01.10.004 | FDA UDI | Class II | Active |
| EXULT Knee Replacement System | KA.ICR.0916-PPX | FDA UDI | Class II | Active |
| LOSPA Knee System | 01.62.025 | FDA UDI | Class II | Active |
| Exult Knee Replacement System Instrument | KA.IUC.0310 | FDA UDI | Class II | Active |
| Exult Knee Replacement System | K3.IDX.4775-14T | FDA UDI | Class II | Active |
| LOSPA Knee System | KD.STT.L910 | FDA UDI | Class II | Active |
| EXULT Knee Replacement System | KA.SFO.0008 | FDA UDI | Class II | Active |
| LOSPA IS Spinal Fixation System | SA.223.7014 | FDA UDI | Class II | Active |
| LOSPA IS Spinal Fixation System | SA.222.7025 | FDA UDI | Class II | Active |
| LOSPA IS Spinal Fixation System | SA.222.7012 | FDA UDI | Class II | Active |
| LOSPA Knee System | 01.62.11G | FDA UDI | Class II | Active |
| LOSPA IS Spinal Fixation System | SA.225.6040 | FDA UDI | Class II | Active |
| LOSPA IS Spinal System | SI.M20.0024 | FDA UDI | Class II | Active |
| BENCOX THR System | HA.01L.4052 | FDA UDI | Class II | Active |
| LOSPA IS Spinal System | SA.R16.0130 | FDA UDI | Class II | Active |
| LOSPA IS Spinal Fixation System | SA.221.6535 | FDA UDI | Class II | Active |
| EXULT Knee Replacement System | K3.ICX.4775P-12T | FDA UDI | Class II | Active |
| Lospa Tkr System | KA.SPS.0416 | FDA UDI | Class I | Active |
| LOSPA IS Spinal System | SI.C50.2110 | FDA UDI | Class I | Active |
| EXULT Knee Replacement System | KA.CFT.R004 | FDA UDI | Class II | Active |
| EXULT Knee Replacement System | KA.IPS.0620 | FDA UDI | Class II | Active |
| EXULT Knee Replacement System | KA.CFT.R013-SUS | FDA UDI | Class II | Active |
| LOSPA Modular Knee System | K4.TH2.0705-ASY | FDA UDI | Class II | Active |
| LOSPA IS Spinal Fixation System | SA.222.8555 | FDA UDI | Class II | Active |
| LOSPA Knee System | 01.62.2G8 | FDA UDI | Class II | Active |
| LOSPA Knee System | KA.SFT.0076 | FDA UDI | Class II | Active |
| LOSPA IS Spinal System | SI.C50.2011 | FDA UDI | Class II | Active |
| LOSPA & LOSPA IS Spinal System | SC.S52.2409 | FDA UDI | Class II | Active |
| LOSPA IS Spinal Fixation System | 01.71.011 | FDA UDI | Class II | Active |
| LOSPA IS Spinal Fixation System | SA.226.7065 | FDA UDI | Class II | Active |
| LOSPA Modular Knee System | K4.FD2.1405-ASY | FDA UDI | Class II | Active |
| LOSPA Modular Knee System | K2.C13.0080 | FDA UDI | Class II | Active |
| LOSPA IS Spinal Fixation System | SA.221.7017 | FDA UDI | Class II | Active |
| EXULT Knee Replacement System | K3.IBN.4775-20T | FDA UDI | Class II | Active |
| LOSPA IS Spinal Fixation System | SA.222.8015 | FDA UDI | Class II | Active |
| LOSPA IS Spinal Fixation System | SA.222.6075 | FDA UDI | Class II | Active |
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FDA Establishments (1)
Establishments registered with the FDA under this company group, matched by name.
- Corentec Co., Ltd. Cheonan Si, Chungnam · KR FEI 3009106092