3tp, LLC
United StatesFDA applicant, unverified
- Devices
- 2
What 3tp, LLC makes
3tp, LLC develops software-based solutions for medical device integration, including a configurable 3TP Software Option for device customization and a 3TP Workspace platform for managing and visualizing medical device data in clinical environments.
The company’s portfolio is regulated under FDA Class II devices and requires 510(k) clearance for individual products. The solutions are listed in the FDA 510(k) registry and are based in the United States.
Catalogue
3TP Software Option Ref K031350
Regimes: 510(k) Registry: 510(k)3TP Workspace Ref K050862
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does 3tp, LLC have in the registry?
The registry currently lists 2 devices for 3tp, LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list 3tp, LLC's devices?
Among its 2 most recently registered devices, 3tp, LLC has devices listed in FDA 510(k) (2 devices).
What risk classes do 3tp, LLC's devices fall under?
Among its 2 most recently registered devices, the classes recorded for 3tp, LLC's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from 3tp, LLC in the registry?
The most recently registered devices listed for 3tp, LLC include 3TP SOFTWARE OPTION and 3TP WORKSPACE.