Data / Medical devices / Hong Kong / Vincent Healthcare Products Limited
Vincent Healthcare Products Limited: FDA-registered device maker in Kowloon, Hong Kong, 2 510(k) clearances
Vincent Healthcare Products Limited is registered with the FDA (registration 3015537026) in Kowloon, Hong Kong. It lists 3 device types. The FDA files 2 510(k) clearances under its listings, the newest dated December 21, 2022. Registered through 2026. FDA data exported November 3, 2026.
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- FDA registration number
- 3015537026
- Address
- Flat/Rm B2, 7/F, Phase 2,hang Fung Industrial Building, 2G Hok Yuen Street, Hung Hom, Kowloon, Hong Kong, 00000
- Owner or operator
- Vincent Healthcare Products Limited (10060808)
- Roles
- Exporter to the US
- First device listed
- June 26, 2019
- Registered through
- 2026
- Brand names listed
- HMEF 1000 Angled, HMEF 1000 Straight, HMEF Midi Angled, HMEF Midi Straight, Inspired Medical Ventilation Breathing Circuit, TECME VHB20 Heated Humidifier
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Circuit, Breathing (W Connector, Adaptor, Y Piece) | CAI | 1 | Exporter to the US | accessdata.fda.gov |
| Filter, Bacterial, Breathing-Circuit | CAH | 2 | Exporter to the US | accessdata.fda.gov |
| Humidifier, Respiratory Gas, (Direct Patient Interface) | BTT | 2 | Exporter to the US | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| December 21, 2022 | K222351 | inspired VHB20 Heated Humidifier | BTT | Substantially Equivalent | Vincent Healthcare Products Limited | accessdata.fda.gov |
| June 24, 1997 | K970102 | FILTER | CAH | Substantially Equivalent | Promedic, Inc. | accessdata.fda.gov |
Compare with other makers
- All makers of Filter, Bacterial, Breathing-Circuit
- All makers of Humidifier, Respiratory Gas, (Direct Patient Interface)
- All makers of Circuit, Breathing (W Connector, Adaptor, Y Piece)
Updated December 21, 2022. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.