Kenmar Medical
Country not established
- Devices
- 1
What Kenmar Medical makes
Kenmar Medical manufactures retractable needle syringes, including a 3cc model designed for single-use injections. These devices incorporate a safety feature to reduce needle-stick injuries during use and disposal.
The company’s retractable needle syringes fall under FDA Class II regulation and are listed via the 510(k) clearance pathway. The devices are intended for use in the United States.
Catalogue
Retractable Needle 3cc Syringe Ref K881454
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Kenmar Medical have in the registry?
The registry currently lists 1 device for Kenmar Medical. Devices recorded under merged duplicate company entries are counted once.
Which registries list Kenmar Medical's devices?
Among its 1 most recently registered device, Kenmar Medical has devices listed in FDA 510(k) (1 device).
What risk classes do Kenmar Medical's devices fall under?
Among its 1 most recently registered device, the classes recorded for Kenmar Medical's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Kenmar Medical in the registry?
The most recently registered devices listed for Kenmar Medical include RETRACTABLE NEEDLE 3CC SYRINGE.