Data / Medical devices / China / V&Q Manufacturing Corporation
V&Q Manufacturing Corporation: FDA-registered device maker in Xiantao Hubei, China, 1 510(k) clearance
V&Q Manufacturing Corporation is registered with the FDA (registration 3007479164) in Xiantao Hubei, China. It lists 14 device types. The FDA files 1 510(k) clearance under its listings, the newest dated January 25, 2018. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3007479164
- FEI number
- 3010322103
- Address
- No. 107 Wagou New District Pengchang, Xiantao Hubei, China, 433018
- Owner or operator
- V&Q Manufacturing Corporation (10028103)
- Roles
- Manufacturer
- First device listed
- December 30, 2008
- Registered through
- 2026
- Brand names listed
- ACCESSORY, SURGICAL APPAREL, Applicator, absorbent tipped, sterile, Apron, protective, BAG, ICE, BEDDING, DISPOSABLE, MEDICAL, CAP, SURGICAL, COVER, CAST, DEPRESSOR, TONGUE, NON-SURGICAL and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Accessory, Surgical Apparel | LYU | 1 | Manufacturer | accessdata.fda.gov |
| Applicator, Absorbent Tipped, Sterile | KXG | 1 | Manufacturer | accessdata.fda.gov |
| Apron, Protective | IWO | 1 | Manufacturer | accessdata.fda.gov |
| Bag, Ice | KYR | 1 | Manufacturer | accessdata.fda.gov |
| Bedding, Disposable, Medical | KME | 1 | Manufacturer | accessdata.fda.gov |
| Cap, Surgical | FYF | 1 | Manufacturer | accessdata.fda.gov |
| Cover, Cast | KIA | 1 | Manufacturer | accessdata.fda.gov |
| Depressor, Tongue, Non-Surgical | FMA | 1 | Manufacturer | accessdata.fda.gov |
| Gauze / Sponge,Nonresorbable For External Use | NAB | 1 | Manufacturer | accessdata.fda.gov |
| Gown, Examination | FME | 1 | Manufacturer | accessdata.fda.gov |
| Mask, Surgical | FXX | 2 | Manufacturer | accessdata.fda.gov |
| Non-Surgical Gown | OEA | 1 | Manufacturer | accessdata.fda.gov |
| Shoe And Shoe Cover, Conductive | BWP | 1 | Manufacturer | accessdata.fda.gov |
| Suit, Surgical | FXO | 1 | 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 |
|---|---|---|---|---|---|---|
| January 25, 2018 | K173062 | Non Woven Face Mask (Models: VQN0185W (earloop) and VQN0185B (ties)) | FXX | Substantially Equivalent | V&Q Manufacturing Corporation | accessdata.fda.gov |
Compare with other makers
- All makers of Suit, Surgical
- All makers of Gauze / Sponge,Nonresorbable For External Use
- All makers of Cap, Surgical
- All makers of Bag, Ice
- All makers of Cover, Cast
- All makers of Depressor, Tongue, Non-Surgical
Updated January 25, 2018. 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.