Data / Medical devices / China / Ningbo HSCC Medical Technology Co., Ltd
Ningbo HSCC Medical Technology Co., Ltd: FDA-registered device maker in Ningbo Zhejiang, China, 2 510(k) clearances
Ningbo HSCC Medical Technology Co., Ltd is registered with the FDA (registration 3008688054) in Ningbo Zhejiang, China. It lists 7 device types. The FDA files 2 510(k) clearances under its listings, the newest dated September 1, 2015. Registered through 2026. FDA data exported November 3, 2026.
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- FDA registration number
- 3008688054
- Address
- No. 56 Luoming South Road, Guanhaiwei Town, Cixi, Ningbo Zhejiang, China, 315316
- Owner or operator
- Ningbo HSCC Medical Technology Co., Ltd (10033893)
- Roles
- Manufacturer
- First device listed
- October 15, 2010
- Registered through
- 2026
- Brand names listed
- A Wall Mounted Canister, EYE CUP, LNS-10GAL, LNS-17GAL, LNS-T1, Medical Face Shield, Medical Isolation Goggles, Non-surgical Mask and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Accessory, Surgical Apparel | LYU | 1 | Manufacturer | accessdata.fda.gov |
| Apparatus, Suction, Operating-Room, Wall Vacuum Powered | GCX | 2 | Manufacturer | accessdata.fda.gov |
| Container, Sharps | MMK | 2 | Manufacturer | accessdata.fda.gov |
| Cup, Eye | LXQ | U | Manufacturer | accessdata.fda.gov |
| Exerciser, Non-Measuring | ION | 1 | Manufacturer | accessdata.fda.gov |
| Shield, Eye, Ophthalmic (Including Sunlamp Protective Eyewear And Post-Mydriatic Eyewear) | HOY | 1 | Manufacturer | accessdata.fda.gov |
| Tubing, Pressure And Accessories | BYX | 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 |
|---|---|---|---|---|---|---|
| September 1, 2015 | K151575 | Dynarex Eye Cups | LXQ | Substantially Equivalent | Dynarex Corporation | accessdata.fda.gov |
| September 2, 2010 | K101567 | SHARPS CONTAINER | MMK | Substantially Equivalent | Cixi Leinuo Plastic Co., Ltd. | accessdata.fda.gov |
Compare with other makers
- All makers of Container, Sharps
- All makers of Accessory, Surgical Apparel
- All makers of Shield, Eye, Ophthalmic (Including Sunlamp Protective Eyewear And Post-Mydriatic Eyewear)
- All makers of Tubing, Pressure And Accessories
- All makers of Exerciser, Non-Measuring
- All makers of Apparatus, Suction, Operating-Room, Wall Vacuum Powered
Updated September 1, 2015. 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.