Data / Medical devices / China / Vincent Medical(dongguan)technology Company Limited
Vincent Medical(dongguan)technology Company Limited: FDA-registered device maker in Dongguan Guangdong, China, 1 510(k) clearance
Vincent Medical(dongguan)technology Company Limited is registered with the FDA (registration 3017235290) in Dongguan Guangdong, China. It lists 2 device types. The FDA files 1 510(k) clearance 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
- 3017235290
- Address
- RM 101 and 201, Block 10, 1st Taoyuan Road, Songshan Lake Zone, Dongguan 523808, Guangdong P.R. China, Dongguan Guangdong, China, 523808
- Owner or operator
- Vincent Medical(Dongguan)Technology Company Limited (10076353)
- Roles
- Contract manufacturer, Manufacturer
- First device listed
- July 11, 2021
- Registered through
- 2026
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Humidifier, Respiratory Gas, (Direct Patient Interface) | BTT | 2 | Manufacturer | accessdata.fda.gov |
| Transilluminator, Battery-Powered | HJN | 1 | Contract manufacturer | 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 |
Compare with other makers
- All makers of Humidifier, Respiratory Gas, (Direct Patient Interface)
- All makers of Transilluminator, Battery-Powered
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.