Data / Medical devices / China / Vega Technologies Inc.
Vega Technologies Inc.: FDA-registered device maker in Dongguan City Guangdong, China, 4 510(k) clearances
Vega Technologies Inc. is registered with the FDA (registration 9616843) in Dongguan City Guangdong, China. It lists 7 device types. The FDA files 4 510(k) clearances under its listings, the newest dated January 14, 2011. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 9616843
- FEI number
- 3003188183
- Address
- No.505, Shengping Mid.Road, Yangwu Dalang Town, Dongguan City Guangdong, China, 523789
- Owner or operator
- VEGA TECHNOLOGIES, INC. (9036509)
- Roles
- Manufacturer, Repackager or relabeler
- First device listed
- March 30, 2001
- Registered through
- 2026
- Brand names listed
- 3-Mode Electronic Fever Cooler(CM-01), Compressor Nebulizer, Digital thermometer, Electric Suction Unit, Medical Nebulizer Kits, Non-contacted Infrared forehead thermometer, Steam Inhalator
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Apparatus, Suction, Ward Use, Portable, Ac-Powered | JCX | 2 | Manufacturer | accessdata.fda.gov |
| Compressor, Air, Portable | BTI | 2 | Manufacturer | accessdata.fda.gov |
| Continuous Measurement Thermometer | FLL | 2 | Manufacturer | accessdata.fda.gov |
| Humidifier, Non-Direct Patient Interface (Home-Use) | KFZ | 1 | Manufacturer | accessdata.fda.gov |
| Mask, Gas, Anesthetic | BSJ | 1 | Manufacturer | accessdata.fda.gov |
| Nebulizer (Direct Patient Interface) | CAF | 2 | Manufacturer | accessdata.fda.gov |
| Pack, Hot Or Cold, Reusable | IME | 1 | Manufacturer, Repackager or relabeler | 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 |
|---|---|---|---|---|---|---|
| January 14, 2011 | K102934 | INFRARED EAR THERMOMETER, MODEL IR-04MT | FLL | Substantially Equivalent | Vega Technologies, Inc. | accessdata.fda.gov |
| November 12, 2010 | K102626 | VEGA MEDICAL SUCTION EQUIPMENT, MODEL SU-01/SU-DC01 | JCX | Substantially Equivalent | Vega Technologies, Inc. | accessdata.fda.gov |
| September 8, 2004 | K041516 | DIGITAL THERMOMETER, MODELS MT-XX8 AND MT-XX9 | FLL | Substantially Equivalent | Vega Technologies, Inc. | accessdata.fda.gov |
| October 7, 2003 | K031413 | VIGORMIST COMPRESSOR NEBULIZER | BTI | Substantially Equivalent | Vega Technologies, Inc. | accessdata.fda.gov |
Compare with other makers
- All makers of Nebulizer (Direct Patient Interface)
- All makers of Compressor, Air, Portable
- All makers of Humidifier, Non-Direct Patient Interface (Home-Use)
- All makers of Apparatus, Suction, Ward Use, Portable, Ac-Powered
- All makers of Continuous Measurement Thermometer
- All makers of Pack, Hot Or Cold, Reusable
Updated January 14, 2011. 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.