Sisan Assoc.
Country not established
- Devices
- 1
What Sisan Assoc. makes
Sisan Assoc. manufactures fracture reduction systems, including the Model OR 1001, designed for orthopedic applications to assist in the alignment of broken bones during surgical procedures.
The company’s fracture reduction systems fall under FDA Class II devices and are listed via the 510(k) pathway. The manufacturer is based in the United States.
Catalogue
Fracture Reduction Sys., Model Or 1001 Ref K770388
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Sisan Assoc. have in the registry?
The registry currently lists 1 device for Sisan Assoc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Sisan Assoc.'s devices?
Among its 1 most recently registered device, Sisan Assoc. has devices listed in FDA 510(k) (1 device).
What risk classes do Sisan Assoc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Sisan Assoc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Sisan Assoc. in the registry?
The most recently registered devices listed for Sisan Assoc. include FRACTURE REDUCTION SYS., MODEL OR 1001.