Corin USA
Country not established
- Devices
- 79
- FDA recalls
- 3
At a glance
Market reach
- United States
- FDA recalls
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 1-50 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.
Full distribution text
- 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.
Frequently asked questions
How many devices does Corin USA have in the registry?
The registry currently lists 79 devices for Corin USA. Devices recorded under merged duplicate company entries are counted once.
Which registries list Corin USA's devices?
Among its 50 most recently registered devices, Corin USA has devices listed in FDA 510(k) (50 devices).
What risk classes do Corin USA's devices fall under?
Among its 50 most recently registered devices, the classes recorded for Corin USA's devices are Class II. Each device page shows its own class and authorisation.
Are there FDA recall records for Corin USA?
FDA recall records list 3 recalls initiated by Corin USA, the most recent initiated on 29 Jan 2016. A recall is often a precaution started by the manufacturer; the records say nothing about the company's overall record.
What are the newest devices from Corin USA in the registry?
The most recently registered devices listed for Corin USA include THE MEHDIAN LUMBO-SACRAL PEDICLE SCREW SYSTEM, CORIN METAFIX HIP STEM, THE LIGAMENT ANCHOR SOFT SCREW and Optimized Positioning System (OPS) ReView.