Konliking Tech & Dev. Limited
ChinaFDA 510(k) applicant, unverified FDA FEI 3014159202
- Devices
- 1
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
What Konliking Tech & Dev. Limited makes
Konliking Tech & Dev. Limited manufactures an Air Compression Therapy Device, specifically the model HW6007, designed for therapeutic compression applications.
The company’s portfolio is regulated under Class II devices in the US and is listed via the FDA’s 510(k) pathway. The manufacturer is based in the United States.
Catalogue
Air Compression Therapy Device, model HW6007 Ref K210240
510(k) 510(k)
Company details
- FDA FEI number
- 3014159202
- Address
- The 3nd Floor, Building 3, Floor 1/2/3, Building 2, Dawang Industrial Zone, Pinghu, Longgang,, Shenzhen Guangdong
Frequently asked questions
How many devices does Konliking Tech & Dev. Limited have in the registry?
The registry currently lists 1 device for Konliking Tech & Dev. Limited. Devices recorded under merged duplicate company entries are counted once.
Which registries list Konliking Tech & Dev. Limited's devices?
Among its 1 most recently registered device, Konliking Tech & Dev. Limited has devices listed in FDA 510(k) (1 device).
What risk classes do Konliking Tech & Dev. Limited's devices fall under?
Among its 1 most recently registered device, the classes recorded for Konliking Tech & Dev. Limited's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Konliking Tech & Dev. Limited in the registry?
The most recently registered devices listed for Konliking Tech & Dev. Limited include Air Compression Therapy Device, model HW6007.