The Traumafuse Co.
Country not established
- Devices
- 4
What The Traumafuse Co. makes
The Traumafuse Co. manufactures medical devices for airway management and fluid resuscitation in critical care, including an endotracheal tube for anesthesia, a perfusion pressure relief valve for trauma patients, a tracheal shield for airway protection, and a rapid infusion device for emergency fluid delivery.
These devices are classified as Class II under FDA regulations and are authorised via the 510(k) pathway. The company is based in the United States.
Catalogue
Connell-Stephens Endo Aness Tube Ref K895132
Regimes: 510(k) Registry: 510(k)Traumafuse Perfusion Pressure Relief Valve Ref K894721
Regimes: 510(k) Registry: 510(k)Traumafuse Trach Shield Ref K895162
Regimes: 510(k) Registry: 510(k)Traumafuse Rapid Infusion Device Ref K890077
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does The Traumafuse Co. have in the registry?
The registry currently lists 4 devices for The Traumafuse Co.. Devices recorded under merged duplicate company entries are counted once.
Which registries list The Traumafuse Co.'s devices?
Among its 4 most recently registered devices, The Traumafuse Co. has devices listed in FDA 510(k) (4 devices).
What risk classes do The Traumafuse Co.'s devices fall under?
Among its 4 most recently registered devices, the classes recorded for The Traumafuse Co.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from The Traumafuse Co. in the registry?
The most recently registered devices listed for The Traumafuse Co. include CONNELL-STEPHENS ENDO ANESS TUBE, TRAUMAFUSE PERFUSION PRESSURE RELIEF VALVE, TRAUMAFUSE TRACH SHIELD and TRAUMAFUSE RAPID INFUSION DEVICE.