American Bentley
Country not established
- Devices
- 59
What American Bentley makes
American Bentley manufactures medical devices for cardiopulmonary bypass and cardioplegia systems, including gasline filters, electrosurgical probes, integrated membrane oxygenators with cardiotomy filters, and oxygen monitoring probes. Their portfolio also covers oxygenator holders, heat exchangers, reservoir bags, and blood filters for arterial and venous circuits, as well as cardiotomy reservoirs with integrated filtration.
The company’s devices are regulated under FDA 510(k) clearance, with products classified as Class I and Class II. These items are listed in the FDA’s 510(k) registry, reflecting their compliance with U.S. medical device regulations. The manufacturer is based in the United States.
Catalogue
Search and filter all 59 devicesShowing 1-50 of 59
Frequently asked questions
How many devices does American Bentley have in the registry?
The registry currently lists 59 devices for American Bentley. Devices recorded under merged duplicate company entries are counted once.
Which registries list American Bentley's devices?
Among its 50 most recently registered devices, American Bentley has devices listed in FDA 510(k) (50 devices).
What risk classes do American Bentley's devices fall under?
Among its 50 most recently registered devices, the classes recorded for American Bentley's devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from American Bentley in the registry?
The most recently registered devices listed for American Bentley include GASLINE FILTER #GF-10, ELECTROSURGICAL LATERAL RELEASE PROBE MOD ALR-100, INTEGRATED MEMBRANE OXYGENATOR W/CARDIOTOMY FILTER and OXYGEN MONITOR NO. OM-100, OXYGEN PROBE NO. OP-100.