Satyrne Medical
Country not established
- Devices
- 1
What Satyrne Medical makes
Satyrne Medical designs the Satyrne Interflex Mandibular Fixation System, a device used for internal fixation of mandibular fractures, providing rigid stabilization to aid bone healing.
The company’s portfolio is regulated under FDA Class II devices, with the Interflex System authorised via the 510(k) pathway. The manufacturer is based in the United States.
Catalogue
Satyrne Interflex Mandibular Fixation System Ref K072463
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Satyrne Medical have in the registry?
The registry currently lists 1 device for Satyrne Medical. Devices recorded under merged duplicate company entries are counted once.
Which registries list Satyrne Medical's devices?
Among its 1 most recently registered device, Satyrne Medical has devices listed in FDA 510(k) (1 device).
What risk classes do Satyrne Medical's devices fall under?
Among its 1 most recently registered device, the classes recorded for Satyrne Medical's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Satyrne Medical in the registry?
The most recently registered devices listed for Satyrne Medical include SATYRNE INTERFLEX MANDIBULAR FIXATION SYSTEM.