Bespoke Technologies
Country not established
- Devices
- 98
What Bespoke Technologies makes
Bespoke Technologies manufactures the Tailored-C Cervical Interbody Fusion System, a spinal implant designed for cervical interbody fusion procedures in the neck region.
The company’s portfolio is regulated under FDA Class II devices and includes submissions via the 510(k) pathway. The manufacturer is based in the United States.
Catalogue
Search and filter all 98 devicesShowing 1-50 of 98
Frequently asked questions
How many devices does Bespoke Technologies have in the registry?
The registry currently lists 98 devices for Bespoke Technologies. Devices recorded under merged duplicate company entries are counted once.
Which registries list Bespoke Technologies's devices?
Among its 50 most recently registered devices, Bespoke Technologies has devices listed in FDA GUDID (50 devices).
What risk classes do Bespoke Technologies's devices fall under?
Among its 50 most recently registered devices, the classes recorded for Bespoke Technologies's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Bespoke Technologies in the registry?
The most recently registered devices listed for Bespoke Technologies include Tailored-H BCS7-1518-6, Tailored-H BCS12-1416-7, Tailored-C BC4-1214-7 and Tailored-H BCSD-4014.