Corin USA
Country not established
- Devices
- 79
- FDA recalls
- 3
What Corin USA makes
Corin USA manufactures orthopedic implant systems including pedicle screw systems for spinal fixation, hip stems such as the Metafix and TaperFit models, acetabular cup systems like the C-Fit and DC-Fit, modular revision hip stems, and total knee systems including the Unity and Nuffield platforms. The company also produces ligament anchoring devices such as the Ligament Anchor Soft Screw and spinal instrumentation including polyaxial screws and rods from the Mehidian Spinal Rod series, along with optimized positioning systems like OPS ReView and OPS Insight for surgical guidance.
The devices manufactured by Corin USA are classified as Class II and Class III medical devices and are listed in the FDA’s 510(k) and Premarket Approval (PMA) registries. The company is based in the United States.
Catalogue
Search and filter all 79 devicesShowing 51-79 of 79
FDA recalls
FDA recall records list 3 recalls initiated by Corin USA, initiated on 2016-01-29. By recorded status: 3 terminated. The reasons filed fall into these groups: sterility or contamination and packaging. A recall is often a precaution started by the manufacturer, and a count of records is not a verdict on a company.
2016
- 29 Jan 2016 Z-1526-2016 Class II Terminated Potential for abrasion of the sterile barrier pouches of the new packaging system.
Full distribution text
- 29 Jan 2016 Z-1527-2016 Class II Terminated Potential for abrasion of the sterile barrier pouches of the new packaging system.
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- 29 Jan 2016 Z-1528-2016 Class II Terminated Potential for abrasion of the sterile barrier pouches of the new packaging system.
Full distribution text
- 29 Jan 2016 Z-1526-2016 Class II Terminated Potential for abrasion of the sterile barrier pouches of the new packaging system.