Data / Medical devices / Multiple Use Blood Lancet For Single Patient Use Only / China
FDA-registered makers of Multiple Use Blood Lancet For Single Patient Use Only in China: 12 establishments
12 establishments in China are registered with the FDA to make Multiple Use Blood Lancet For Single Patient Use Only (product code QRL). 7 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 3, 2026.
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- Device
- Multiple Use Blood Lancet For Single Patient Use Only
- Product code
- QRL
- Country
- China
Makers of Multiple Use Blood Lancet For Single Patient Use Only in China
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Tianjin Huahong Technology Co., Ltd. | Tianjin, China | Contract manufacturer, Manufacturer | 3 | December 9, 2025 | 0 | 0 | 0 | api.fda.gov |
| Sterilance Medical (Suzhou) Inc. | Suzhou Jiangsu, China | Contract manufacturer, Exporter to the US, Manufacturer | 2 | July 6, 2026 | 0 | 0 | 0 | api.fda.gov |
| Beijing Ruicheng Medical Supplies Co., Ltd. | Beijing, China | Manufacturer | 1 | September 7, 2022 | 0 | 0 | 0 | api.fda.gov |
| Promisemed Hangzhou Meditech Co.,ltd. | Hangzhou Zhejiang, China | Exporter to the US, Manufacturer | 1 | February 21, 2023 | 0 | 0 | 0 | api.fda.gov |
| Shandong Lianfa Medical Plastic Products Co. Ltd. | JINAN Shandong, China | Manufacturer | 1 | November 30, 2022 | 0 | 0 | 0 | api.fda.gov |
| Suzhou Kyuan Medical Apparatus Co., Ltd. | Suzhou City Jiangsu, China | Manufacturer | 1 | August 17, 2022 | 0 | 0 | 0 | api.fda.gov |
| Tianjin Rilifine Medical Device Co.,ltd | Tianjin, China | Manufacturer | 1 | November 21, 2022 | 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 | 0 | 0 | 0 | 0 | api.fda.gov | |
| Jetcrown Industrial (dong Guan) Ltd. | Guangdong Province, China | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Ningbo Caremed Medical Products Co Ltd | Ningbo Zhejiang, China | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Ningbo Chibanda Imp &exp Co, Ltd | Ningbo Zhejiang, China | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Ningbo Medsun Medical Co., Ltd. | Ningbo Zhejiang, China | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov |
Updated November 3, 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.