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Sign in to claim this brandRootLoc Co., Ltd.
US
Last updated May 23, 2026
What RootLoc Co., Ltd. makes
RootLoc Co., Ltd. manufactures femur and tibia shaft prostheses, specialising in the CentLoc Total Knee System—a modular knee replacement designed for primary total knee arthroplasty. The system includes components intended to restore joint function and alignment in patients with degenerative joint disease or trauma-related knee damage.
The company’s products are classified as Class II medical devices under FDA regulations and are listed in the FDA’s Unique Device Identifier (UDI) database. The manufacturer operates from the United States, adhering to applicable U.S. regulatory requirements for orthopaedic implants.
Written from this company's registered devices by an AI model, and not verified by a human reviewer.
Information
- Country
- US
- Address
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- Website
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- Phone
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- PRRC Contact
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- EUDAMED SRN
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- FDA FEI Number
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- DUNS Number
- 694670830
Catalogue (467)
Page 10 of 10| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| CentLoc Total Knee System | 7121-4771 | FDA UDI | Class II | Active |
| CentLoc Total Knee System | 7131-0909 | FDA UDI | Class II | Active |
| CentLoc Total Knee System | 7131-0115 | FDA UDI | Class II | Active |
| CentLoc Total Knee System | 7132-1517 | FDA UDI | Class II | Active |
| CentLoc Total Knee System | 7131-1816 | FDA UDI | Class II | Active |
| CentLoc Total Knee System | 7131-0416 | FDA UDI | Class II | Active |
| CentLoc Total Knee System | 7131-0612 | FDA UDI | Class II | Active |
| CentLoc Total Knee System | 7131-1210 | FDA UDI | Class II | Active |
| CentLoc Total Knee System | 7131-0315 | FDA UDI | Class II | Active |
| CentLoc Total Knee System | 7132-1609 | FDA UDI | Class II | Active |
| CentLoc Total Knee System | 7132-0513 | FDA UDI | Class II | Active |
| CentLoc Total Knee System | 7131-0515 | FDA UDI | Class II | Active |
| CentLoc Total Knee System | 7131-0412 | FDA UDI | Class II | Active |
| CentLoc Total Knee System | 7132-1313 | FDA UDI | Class II | Active |
| CentLoc Total Knee System | 7111-7680R | FDA UDI | Class II | Active |
| Acculoc Total Knee System | K170753 | FDA 510(k) | Class II | Active |
| Acculoc Total Knee System | K182370 | FDA 510(k) | Class II | Active |
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