Oratronics, Inc.
Country not established
- Devices
- 1
What Oratronics, Inc. makes
Oratronics, Inc. manufactures endosseous frame assemblies, which are orthopedic implants designed to stabilize and support bone structures, commonly used in spinal or limb reconstruction 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
Oratronics Endosseous Frame Assembly Ref K791366
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Oratronics, Inc. have in the registry?
The registry currently lists 1 device for Oratronics, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Oratronics, Inc.'s devices?
Among its 1 most recently registered device, Oratronics, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Oratronics, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Oratronics, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Oratronics, Inc. in the registry?
The most recently registered devices listed for Oratronics, Inc. include ORATRONICS ENDOSSEOUS FRAME ASSEMBLY.