Bpendo, LLC
United StatesFDA 510(k) applicant, unverified
- Devices
- 2
Catalogue
- 510(k) 510(k)
Insufflation Retention Device Ref K213773
510(k) 510(k)
Frequently asked questions
How many devices does Bpendo, LLC have in the registry?
The registry currently lists 2 devices for Bpendo, LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list Bpendo, LLC's devices?
Among its 2 most recently registered devices, Bpendo, LLC has devices listed in FDA 510(k) (2 devices).
What risk classes do Bpendo, LLC's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Bpendo, LLC's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Bpendo, LLC in the registry?
The most recently registered devices listed for Bpendo, LLC include Insufflation Retention Device (IRD) (11173-325-101) and Insufflation Retention Device.