Data / Medical devices / China / Beijing Ruicheng Medical Supplies Co., Ltd.
Beijing Ruicheng Medical Supplies Co., Ltd.: FDA-registered device maker in Beijing, China, 2 510(k) clearances
Beijing Ruicheng Medical Supplies Co., Ltd. is registered with the FDA (registration 3008191276) in Beijing, China. It lists 4 device types. The FDA files 2 510(k) clearances under its listings, the newest dated November 29, 2022. Registered through 2026. FDA data exported November 3, 2026.
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- FDA registration number
- 3008191276
- Address
- Building 5, No. 8, Yanqi West Road, Yanqi Economic Development Zone, Huairou District, Beijing, China, 101407
- Owner or operator
- Beijing Ruicheng Medical Supplies Co., Ltd. (10031145)
- Roles
- Contract manufacturer, Exporter to the US, Manufacturer
- First device listed
- December 23, 2009
- Registered through
- 2026
- Brand names listed
- Alcohol Prep Pad, CareSens Lancing device, CareSoft Lancing Device, Clever Choice Alcohol Prep Pads, Clever Choice Lancet Device, Clever Choice Lancets, DS-A, DS-W and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Gauze / Sponge,Nonresorbable For External Use | NAB | 1 | Contract manufacturer, Exporter to the US, Manufacturer | accessdata.fda.gov |
| Multiple Use Blood Lancet For Single Patient Use Only | QRL | 2 | Manufacturer | accessdata.fda.gov |
| Single Use Only Blood Lancet With An Integral Sharps Injury Prevention Feature | FMK | 2 | Manufacturer | accessdata.fda.gov |
| Single Use Only Blood Lancet Without An Integral Sharps Injury Prevention Feature | QRK | 2 | 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 |
|---|---|---|---|---|---|---|
| November 29, 2022 | K222408 | Disposable Safety Lancet | FMK | Substantially Equivalent | Beijing Ruicheng Medical Supplies Co., Ltd. | accessdata.fda.gov |
| September 7, 2022 | K222034 | RightLance Blood Lancing System | QRL | Substantially Equivalent | Beijing Ruicheng Medical Supplies Co., Ltd. | accessdata.fda.gov |
Compare with other makers
- All makers of Multiple Use Blood Lancet For Single Patient Use Only
- All makers of Single Use Only Blood Lancet Without An Integral Sharps Injury Prevention Feature
- All makers of Single Use Only Blood Lancet With An Integral Sharps Injury Prevention Feature
- All makers of Gauze / Sponge,Nonresorbable For External Use
Updated November 29, 2022. 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.