Data / Medical devices / China / Vastrade Manufacturing Corporation
Vastrade Manufacturing Corporation: FDA-registered device maker in Shenzhen Guangdong, China, 2 510(k) clearances
Vastrade Manufacturing Corporation is registered with the FDA (registration 3009155880) in Shenzhen Guangdong, China. It lists 18 device types. The FDA files 2 510(k) clearances under its listings, the newest dated November 26, 2004. Registered through 2026. FDA data exported November 3, 2026.
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- FDA registration number
- 3009155880
- Address
- Building 26, Tongfuyu Industrial Zone, Longtian Community, Longtian Street, PingShan District, Shenzhen Guangdong, China, 518100
- Owner or operator
- Vastrade Manufacturing Corporation (10036268)
- Roles
- Contract manufacturer, Exporter to the US, Manufacturer, Repackager or relabeler
- First device listed
- April 27, 2011
- Registered through
- 2026
- Brand names listed
- COVER, CAST, DETECTORS AND REMOVERS, LICE, (INCLUDING COMBS), DEVICE, ACUPRESSURE, DISPENSER, LIQUID MEDICATION, Device, Acupressure, Dressing, wound, occlusive, FIBER, MEDICAL, ABSORBENT, Face Shield and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Cover, Cast | KIA | 1 | Contract manufacturer, Exporter to the US, Manufacturer, Repackager or relabeler | accessdata.fda.gov |
| Detectors And Removers, Lice, (Including Combs) | LJL | 1 | Contract manufacturer, Exporter to the US, Manufacturer, Repackager or relabeler | accessdata.fda.gov |
| Device, Acupressure | MVV | U | Contract manufacturer, Exporter to the US, Manufacturer, Repackager or relabeler | accessdata.fda.gov |
| Dispenser, Liquid Medication | KYX | 1 | Contract manufacturer, Exporter to the US, Manufacturer, Repackager or relabeler | accessdata.fda.gov |
| Dispenser, Solid Medication | NXB | 1 | Contract manufacturer, Exporter to the US, Manufacturer, Repackager or relabeler | accessdata.fda.gov |
| Dressing, Wound, Occlusive | NAD | 1 | Contract manufacturer, Exporter to the US, Manufacturer, Repackager or relabeler | accessdata.fda.gov |
| Fiber, Medical, Absorbent | FRL | 1 | Contract manufacturer, Exporter to the US, Manufacturer, Repackager or relabeler | accessdata.fda.gov |
| Gauze / Sponge,Nonresorbable For External Use | NAB | 1 | Contract manufacturer, Exporter to the US, Manufacturer, Repackager or relabeler | accessdata.fda.gov |
| Joint, Ankle, External Brace | ITW | 1 | Contract manufacturer, Exporter to the US, Manufacturer, Repackager or relabeler | accessdata.fda.gov |
| Massager, Therapeutic, Manual | LYG | 1 | Contract manufacturer, Exporter to the US, Manufacturer, Repackager or relabeler | accessdata.fda.gov |
| Otoscope | ERA | 1 | Contract manufacturer, Exporter to the US, Manufacturer, Repackager or relabeler | accessdata.fda.gov |
| Pack, Hot Or Cold, Reusable | IME | 1 | Contract manufacturer, Exporter to the US, Manufacturer, Repackager or relabeler | accessdata.fda.gov |
| Pill Crusher/Cutter | OHY | 1 | Contract manufacturer, Exporter to the US, Manufacturer, Repackager or relabeler | accessdata.fda.gov |
| Shield, Eye, Ophthalmic (Including Sunlamp Protective Eyewear And Post-Mydriatic Eyewear) | HOY | 1 | Contract manufacturer, Exporter to the US, Manufacturer, Repackager or relabeler | accessdata.fda.gov |
| Splint, Hand, And Components | ILH | 1 | Contract manufacturer, Exporter to the US, Manufacturer, Repackager or relabeler | accessdata.fda.gov |
| Spoon, Ear | JZE | 1 | Contract manufacturer, Exporter to the US, Manufacturer, Repackager or relabeler | accessdata.fda.gov |
| Syringe, Ent | KCP | 1 | Contract manufacturer, Exporter to the US, Manufacturer, Repackager or relabeler | accessdata.fda.gov |
| Syringe, Irrigating (Non Dental) | KYZ | 1 | Contract manufacturer, Exporter to the US, 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 |
|---|---|---|---|---|---|---|
| November 26, 2004 | K041766 | EZY-TRAVEL WRISTBAND | MVV | Substantially Equivalent | Apothecary Products, Inc. | accessdata.fda.gov |
| October 8, 2004 | K041877 | ACU-STRAP MOTION SICKNESS BAND | MVV | Substantially Equivalent | Health Ent., Inc. | accessdata.fda.gov |
Compare with other makers
- All makers of Device, Acupressure
- All makers of Dressing, Wound, Occlusive
- All makers of Splint, Hand, And Components
- All makers of Dispenser, Solid Medication
- All makers of Syringe, Ent
- All makers of Gauze / Sponge,Nonresorbable For External Use
Updated November 26, 2004. 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.