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Sign in to claim this brandCORIN LTD
US
Last updated May 24, 2026
What CORIN LTD makes
Corin Ltd manufactures reusable orthopaedic instruments for prosthesis implantation positioning, including tibial inserts, acetabular shells, and acetabulum trial prostheses. Their portfolio also includes modular hip femur prostheses, acetabular reamers, knee tibia trial prostheses, and non-constrained polyethylene acetabular liners, as well as modular knee systems with fixed meniscus components.
These devices are classified as Class II under FDA regulations and are listed in the FDA’s Unique Device Identifier (UDI) database. The company operates from the United States.
Written from this company's registered devices by an AI model, and not verified by a human reviewer.
Frequently asked questions
What types of medical devices does Corin Ltd manufacture?
Corin Ltd specializes in orthopaedic devices primarily used in joint replacement surgeries. Their portfolio includes reusable instruments for positioning orthopaedic prostheses, such as tibial inserts and acetabular shells. They also produce modular hip prostheses (e.g., femoral components and acetabular liners), acetabular reamers, trial prostheses for both hip and knee, and modular knee systems with fixed meniscus components. These devices are designed to aid in precise surgical implantation and improve joint function.
Where is Corin Ltd based, and does that affect the regulatory landscape for their devices?
Corin Ltd is based in the United States. Since their devices are classified as Class II under FDA regulations, they must comply with U.S. regulatory requirements, including listing in the FDA’s Unique Device Identifier (UDI) database. This classification reflects a moderate risk level, requiring specific controls to ensure safety and effectiveness. The U.S. regulatory framework applies directly to their products due to their manufacturing location.
Are Corin Ltd’s devices listed in any regulatory registries, and why does this matter?
Yes, Corin Ltd’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. This registry is critical because it provides transparent, standardized identification for medical devices, ensuring traceability, compliance tracking, and easier monitoring by healthcare providers, regulators, and patients. Listing in the UDI system helps streamline post-market surveillance and reduces errors in device identification during clinical use.
How are Corin Ltd’s orthopaedic devices classified under FDA regulations, and what does this classification imply?
Corin Ltd’s devices fall under Class II classification by the FDA, which indicates a moderate risk to patients. This classification requires special controls beyond general controls (like good manufacturing practices) to ensure safety and effectiveness. While not as stringent as Class III (high-risk) devices, Class II still demands validation of performance, labeling requirements, and post-market surveillance to mitigate potential risks associated with orthopaedic implants, such as improper sizing or material compatibility issues.
What role do reusable instruments like those from Corin Ltd play in orthopaedic surgery?
Reusable orthopaedic instruments, such as those manufactured by Corin Ltd (e.g., acetabular reamers or trial prostheses), are essential for precise surgical planning and execution. These tools allow surgeons to test-fit components before final implantation, reducing errors in prosthesis alignment and improving outcomes. By being reusable, they also contribute to cost efficiency and sustainability in healthcare settings, though they must undergo rigorous cleaning and sterilization protocols to maintain safety and functionality between uses.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
- Address
- —
- Website
- coringroup.com
- —
- —
- [email protected]
- Phone
- +330456608978
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- —
- DUNS Number
- 295437313
Catalogue (4152)
Page 11 of 84| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Unity Total Knee System | 123.368.09 | FDA UDI | Class II | Active |
| Unity Total Knee System | 112.014.26 | FDA UDI | Class II | Active |
| HLS Noetos Revision | GDF566 | FDA UDI | Class II | Active |
| Optimom Modular Heads | E279.517 | FDA UDI | Class II | Active |
| MiniHip Stem | 580.0005 | FDA UDI | Class II | Active |
| U-KneeTec | MVV620 | FDA UDI | Class II | Active |
| Rotaglide+ Modular Knee System with Fixed Meniscus | 217.252 | FDA UDI | Class II | Active |
| MobiliT Cup | HDM764 | FDA UDI | Class II | Active |
| HLS KneeTec | MDI224 | FDA UDI | Class II | Active |
| MiniHip Stem | 580.9041.03 | FDA UDI | Class II | Active |
| HLS Noetos | MDF224 | FDA UDI | Class II | Active |
| HLS Noetos | GDF444 | FDA UDI | Class II | Active |
| Unity Total Knee System | 1125246 | FDA UDI | Class II | Active |
| Rotaglide+ Modular Knee System with Fixed Meniscus | 202.904 | FDA UDI | Class II | Active |
| Unity Total Knee System | 123.467.18 | FDA UDI | Class II | Active |
| Trinity Acetabular Hip System with HXLPE Liners | 321.03.636 | FDA UDI | Class II | Active |
| HLS Noetos | MDF012 | FDA UDI | Class II | Active |
| Unity Total Knee System | 1120860 | FDA UDI | Class II | Active |
| HLS Noetos | MDF236 | FDA UDI | Class II | Active |
| Unity Total Knee System | 123.468.13 | FDA UDI | Class II | Active |
| Unity Total Knee System | 112.130.12 | FDA UDI | Class II | Active |
| Unity Total Knee System | 1231097 | FDA UDI | Class II | Active |
| Unity Total Knee System | 123.368.03 | FDA UDI | Class II | Active |
| Unity Total Knee System | 1120762 | FDA UDI | Class II | Active |
| Corifix Ligament Anchor Soft Screw | 408.835 | FDA UDI | Class II | Active |
| Corin Metafix Hip Stem | A340.416 | FDA UDI | Class II | Active |
| Trinity Acetabular Hip System | 9210045 | FDA UDI | Class II | Active |
| HLS Noetos Revision | MDF593 | FDA UDI | Class II | Active |
| HLS KneeTec | GDI004 | FDA UDI | Class II | Active |
| Cormet 2000 Hemi-Hip Metallic Resurfacing Prosthesis | S299.750 | FDA UDI | Class II | Active |
| Unity Total Knee System | 112.130.28 | FDA UDI | Class II | Active |
| C-Fit Femoral Hip System | 124.616 | FDA UDI | Class II | Active |
| Metafix Hip Stem | 579.11069999999995 | FDA UDI | Class II | Active |
| TriFit TS Blade Stem | 694.0008 | FDA UDI | Class II | Active |
| Cormet 2000 Hemi-Hip Metallic Resurfacing Prosthesis | 379.139 | FDA UDI | Class II | Active |
| Rotaglide+ Modular Knee System with Fixed Meniscus | 102.110 | FDA UDI | Class II | Active |
| Unity Total Knee System | 112.017.22 | FDA UDI | Class II | Active |
| HLS Uni Evolution | GDU534 | FDA UDI | Class II | Active |
| Unity Total Knee System | 123.053.00 | FDA UDI | Class II | Active |
| Corin BiPolar-i | 2110051 | FDA UDI | Class II | Active |
| Metafix Hip Stem | 579.2109 | FDA UDI | Class II | Active |
| Cenator Total Hip System | 116.222 | FDA UDI | Class II | Active |
| Cormet 2000 Hemi-Hip Metallic Resurfacing Prosthesis | 379.076 | FDA UDI | Class II | Active |
| Cormet 2000 Hemi-Hip Metallic Resurfacing Prosthesis | 379.096 | FDA UDI | Class II | Active |
| Cormet 2000 Hemi-Hip Metallic Resurfacing Prosthesis | 279.022 | FDA UDI | Class II | Active |
| Corin Bipolar Prosthesis | E011.754 | FDA UDI | Class II | Active |
| Trinity Acetabular Hip System | 921.02.348 | FDA UDI | Class II | Active |
| Unity Total Knee System | 112.001.24 | FDA UDI | Class II | Active |
| Corin Trinity™ PLUS Acetabular Shell | 324.05.768 | FDA UDI | Class II | Active |
| Unity Total Knee System | 123.369.37 | FDA UDI | Class II | Active |
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FDA Establishments (1)
Establishments registered with the FDA under this company group, matched by name.
- Corin Limited CIRENCESTER Gloucestershire · GB FEI 3002806725