Roger Cestac & Assoc.
Country not established
- Devices
- 2
What Roger Cestac & Assoc. makes
Roger Cestac & Assoc. manufactures multitubular thoracic air splints and associated splinting kits designed for immobilizing the rib cage and thoracic region in trauma or surgical settings. These devices are intended to stabilize the chest wall during transport or treatment to prevent further injury.
The company’s products fall under Class I medical devices in the U.S. regulatory framework, with relevant devices listed via FDA 510(k) clearance. The manufacturer operates from the United States.
Catalogue
Multitubular Thoracic Air Splints Ref K811750
Regimes: 510(k) Registry: 510(k)Multitubular Air Splint Kit Ref K811704
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Roger Cestac & Assoc. have in the registry?
The registry currently lists 2 devices for Roger Cestac & Assoc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Roger Cestac & Assoc.'s devices?
Among its 2 most recently registered devices, Roger Cestac & Assoc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Roger Cestac & Assoc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Roger Cestac & Assoc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Roger Cestac & Assoc. in the registry?
The most recently registered devices listed for Roger Cestac & Assoc. include MULTITUBULAR THORACIC AIR SPLINTS and MULTITUBULAR AIR SPLINT KIT.