Stanmore Worldwide Implants, Ltd.
Country not established
- Devices
- 1
What Stanmore Worldwide Implants, Ltd. makes
Stanmore Worldwide Implants, Ltd. manufactures patient-specific total knee replacement implants designed for customised joint arthroplasty procedures.
These devices are classified as Class II under FDA regulations and are listed via the 510(k) clearance process. The company is based in the United States.
Catalogue
Patient Specific Smiles Total Knee Replacement Ref K140900
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Stanmore Worldwide Implants, Ltd. have in the registry?
The registry currently lists 1 device for Stanmore Worldwide Implants, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Stanmore Worldwide Implants, Ltd.'s devices?
Among its 1 most recently registered device, Stanmore Worldwide Implants, Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Stanmore Worldwide Implants, Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Stanmore Worldwide Implants, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Stanmore Worldwide Implants, Ltd. in the registry?
The most recently registered devices listed for Stanmore Worldwide Implants, Ltd. include PATIENT SPECIFIC SMILES TOTAL KNEE REPLACEMENT.