Vincent Healthcare Products Limited
Hong Kong SAR ChinaFDA applicant, unverified FDA FEI 3015537026
- Devices
- 4
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
Catalogue
- Registry: GUDID
- Registry: GUDID
inspired™ Heated Breathing Circuit (510-008) Ref K252066
Regimes: 510(k) Registry: 510(k)inspired™ VHB20 Heated Humidifier Ref K222351
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3015537026
- DUNS number
- 664763919
- Address
- FLAT/RM B2, 7/F, PHASE 2,HANG FUNG INDUSTRIAL BUILDING,, KOWLOON
Frequently asked questions
How many devices does Vincent Healthcare Products Limited have in the registry?
The registry currently lists 4 devices for Vincent Healthcare Products Limited. Devices recorded under merged duplicate company entries are counted once.
Which registries list Vincent Healthcare Products Limited's devices?
Among its 4 most recently registered devices, Vincent Healthcare Products Limited has devices listed in FDA 510(k) (2 devices) and FDA GUDID (2 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Vincent Healthcare Products Limited's devices fall under?
Among its 4 most recently registered devices, the classes recorded for Vincent Healthcare Products Limited's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Vincent Healthcare Products Limited in the registry?
The most recently registered devices listed for Vincent Healthcare Products Limited include inspired™ VHB20, TECME VHB20, inspired™ Heated Breathing Circuit (510-008) and inspired™ VHB20 Heated Humidifier.