Data / Medical devices / China / Vistar Medical Supplies Co., Ltd.
Vistar Medical Supplies Co., Ltd.: FDA-registered device maker in SHENZHEN Guangdong, China, 3 510(k) clearances
Vistar Medical Supplies Co., Ltd. is registered with the FDA (registration 3012360512) in SHENZHEN Guangdong, China. It lists 11 device types. The FDA files 3 510(k) clearances under its listings, the newest dated June 25, 2026. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3012360512
- Address
- 101,201 &301, No.5 Facility, Datianyang Nansi Rd. Dongfang Community, Songgang Street, Bao'an District, SHENZHEN Guangdong, China, 518105
- Owner or operator
- Vistar Medical Supplies Co., Ltd. (10050527)
- Roles
- Contract manufacturer, Manufacturer
- First device listed
- November 29, 2015
- Registered through
- 2026
- Brand names listed
- Air hoses,Adapters,Protective sleeve, Air hoses,adapters, DVT Garment, Disposable Blood Pressure Cuff, Disposable Masks, KN95 Mask, Disposable strapping tourniquet non pneumatic, ELERA Reusable Blood Pressure Cuff-VD-001,VD-002,VD-003,VD-004,VD-005,VD-006,VD-021,VD-022,VD-023,VD-024,VD-025,VD-026, Emergency Tourniquet with Buckle nonpneumatic and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Blood Pressure Cuff | DXQ | 2 | Manufacturer | accessdata.fda.gov |
| Face Mask Within The Scope Of The Face Mask And Barrier Face Covering Enforcement Policy Or Face Mask Umbrella Eua | QKR | N | Manufacturer | accessdata.fda.gov |
| General Use Pneumatic Tourniquet | QGX | 1 | Contract manufacturer, Manufacturer | accessdata.fda.gov |
| Infusor, Pressure, For I.V. Bags | KZD | 1 | Contract manufacturer, Manufacturer | accessdata.fda.gov |
| Lung Sound Monitor | OCR | 2 | Contract manufacturer, Manufacturer | accessdata.fda.gov |
| Mask, Scavenging | KHA | 1 | Contract manufacturer, Manufacturer | accessdata.fda.gov |
| Respirator, Surgical | MSH | 2 | Contract manufacturer, Manufacturer | accessdata.fda.gov |
| Shield, Eye, Ophthalmic (Including Sunlamp Protective Eyewear And Post-Mydriatic Eyewear) | HOY | 1 | Manufacturer | accessdata.fda.gov |
| Sleeve, Limb, Compressible | JOW | 2 | Manufacturer | accessdata.fda.gov |
| Suit, Surgical | FXO | 1 | Manufacturer | accessdata.fda.gov |
| Tourniquet, Nonpneumatic | GAX | 1 | Contract manufacturer, 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 |
|---|---|---|---|---|---|---|
| June 25, 2026 | K253386 | DVT Garment | JOW | Substantially Equivalent | Vistar Medical Supplies Co., Ltd. | accessdata.fda.gov |
| October 29, 2015 | K152468 | Reusable Blood Pressure Cuff | DXQ | Substantially Equivalent | Shenzhen Vistar Medical Supplies Co., Ltd. | accessdata.fda.gov |
| October 29, 2015 | K152465 | Disposable Blood Pressure Cuff | DXQ | Substantially Equivalent | Shenzhen Vistar Medical Supplies Co., Ltd. | accessdata.fda.gov |
Compare with other makers
- All makers of Blood Pressure Cuff
- All makers of General Use Pneumatic Tourniquet
- All makers of Face Mask Within The Scope Of The Face Mask And Barrier Face Covering Enforcement Policy Or Face Mask Umbrella Eua
- All makers of Infusor, Pressure, For I.V. Bags
- All makers of Suit, Surgical
Updated June 25, 2026. 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.