Data / Medical devices / Single Use Only Blood Lancet Without An Integral Sharps Injury Prevention Feature / China
FDA-registered makers of Single Use Only Blood Lancet Without An Integral Sharps Injury Prevention Feature in China: 12 establishments
12 establishments in China are registered with the FDA to make Single Use Only Blood Lancet Without An Integral Sharps Injury Prevention Feature (product code QRK). 5 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 2, 2026.
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- Device
- Single Use Only Blood Lancet Without An Integral Sharps Injury Prevention Feature
- Product code
- QRK
- Country
- China
Makers of Single Use Only Blood Lancet Without An Integral Sharps Injury Prevention Feature in China
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Sterilance Medical (Suzhou) Inc. | Suzhou Jiangsu, China | Contract manufacturer, Manufacturer | 4 | August 25, 2026 | 0 | 0 | 0 | api.fda.gov |
| Ningbo Caremed Medical Products Co Ltd | Ningbo Zhejiang, China | Manufacturer | 2 | October 28, 2024 | 0 | 0 | 0 | api.fda.gov |
| HUAIAN HENING MEDICAL INSTRUMENTS CO., LTD and its Subsidiary HUAIAN JUNRAN IMP.&EXP. TRADING CO.,LTD | Huaian Jiangsu, China | Exporter to the US, Manufacturer | 1 | January 25, 2023 | 0 | 0 | 0 | api.fda.gov |
| Ningbo Medsun Medical Co., Ltd. | Ningbo Zhejiang, China | Manufacturer | 1 | January 4, 2024 | 0 | 0 | 0 | api.fda.gov |
| Shanghai Carelife International Trading Co. Ltd | Jinqiao Pudong Shanghai, China | Exporter to the US, Specification developer | 1 | September 21, 2022 | 0 | 0 | 0 | api.fda.gov |
| Beijing Ruicheng Medical Supplies Co., Ltd. | Beijing, China | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Jetcrown Industrial (dong Guan) Ltd. | Guangdong Province, China | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Promisemed Hangzhou Meditech Co.,ltd. | Hangzhou Zhejiang, China | Exporter to the US, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Shandong Lianfa Medical Plastic Products Co. Ltd. | JINAN Shandong, China | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Suzhou Kyuan Medical Apparatus Co., Ltd. | Suzhou City Jiangsu, China | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Tianjin Rilifine Medical Device Co.,ltd | Tianjin, China | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Tianjin Huahong Technology Co., Ltd. | Tianjin, China | Contract manufacturer, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov |
Updated November 2, 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.