Needlesmart Limited
United KingdomFDA applicant, unverified
- Devices
- 1
What Needlesmart Limited makes
Needlesmart Limited manufactures the NeedleSmart Professional (NS Pro), a safety-engineered needle device designed to reduce needle-stick injuries in healthcare settings by incorporating an automated retraction mechanism.
The NeedleSmart Professional is classified as a Class II medical device in the US and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
NeedleSmart Professional (NS Pro) Ref K202073
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Needlesmart Limited have in the registry?
The registry currently lists 1 device for Needlesmart Limited. Devices recorded under merged duplicate company entries are counted once.
Which registries list Needlesmart Limited's devices?
Among its 1 most recently registered device, Needlesmart Limited has devices listed in FDA 510(k) (1 device).
What risk classes do Needlesmart Limited's devices fall under?
Among its 1 most recently registered device, the classes recorded for Needlesmart Limited's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Needlesmart Limited in the registry?
The most recently registered devices listed for Needlesmart Limited include NeedleSmart Professional (NS Pro).