Hubly, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Hubly, Inc. makes
Hubly, Inc. manufactures the Hubly Drill, also known as the H100, which is an electric surgical drill.
The company is based in the United States, and its devices are classified as Class II medical products that are listed in the FDA 510(k) regulatory registry.
Catalogue
Hubly Drill (H100) Ref K250815
Regimes: 510(k) Registry: 510(k)Hubly Electric Drill (H100) Ref K230619
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Hubly, Inc. have in the registry?
The registry currently lists 2 devices for Hubly, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Hubly, Inc.'s devices?
Among its 2 most recently registered devices, Hubly, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Hubly, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Hubly, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Hubly, Inc. in the registry?
The most recently registered devices listed for Hubly, Inc. include Hubly Drill (H100) and Hubly Electric Drill (H100).