Data / Medical devices / Low Dead Space Piston Syringe
Low Dead Space Piston Syringe (QNQ): 12 FDA-registered makers in 6 countries
12 establishments in 6 countries are registered with the FDA to make Low Dead Space Piston Syringe (product code QNQ, Class 2, 21 CFR 880.5860). 6 of them have a 510(k) clearance or PMA approval on file and 0 have a recall event. The FDA has issued 12 510(k) clearances under this code, the latest on February 19, 2026, and lists 0 recall events (0 Class I). FDA data exported November 2, 2026.
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- Product code
- QNQ
- Device class
- 2
- Regulation
- 880.5860
- Medical specialty
- General Hospital
Makers by country
| Country | Makers |
|---|---|
| China | 4 |
| South Korea | 3 |
| United States | 2 |
| Singapore | 1 |
| United Kingdom | 1 |
| Cambodia | 1 |
Makers of Low Dead Space Piston Syringe
Registered establishments that manufacture, contract manufacture, remanufacture, reprocess or own the specification of this device, with the 510(k) clearances, PMA approvals and recalls the FDA files under each. Best documented first.
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Anhui Hongyu Wuzhou Medical Manufacturer Co., Ltd. | Taihu Anhui, China | Exporter to the US, Manufacturer | 1 | May 25, 2022 | 0 | 0 | 0 | api.fda.gov |
| CMT Health Pte. Ltd. | Singapore, Singapore | Specification developer | 1 | February 19, 2026 | 0 | 0 | 0 | api.fda.gov |
| Feeltech Co.,ltd. | Gunsan-si Jeonbuk, South Korea | Complaint file establishment, Manufacturer | 1 | May 31, 2023 | 0 | 0 | 0 | api.fda.gov |
| Jeil Tech Co.,ltd | Sejong-si Daegu, South Korea | Manufacturer | 1 | September 19, 2022 | 0 | 0 | 0 | api.fda.gov |
| Prosum Medical Limited | London London, City of, United Kingdom | Specification developer | 1 | April 2, 2025 | 0 | 0 | 0 | api.fda.gov |
| Sol-Millennium Medical, Inc. | Chicago, IL, United States | Complaint file establishment, Specification developer | 1 | November 20, 2024 | 0 | 0 | 0 | api.fda.gov |
| Camedical Technology (cambodia) Co., Ltd. | Samraong Takeo, Cambodia | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| HLB Life Science Co., Ltd. | Anseong-si, Gyeonggi-do, South Korea | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Ocuject, LLC | San Diego, CA, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Shanghai Kindly Enterprise Development Group Co., Ltd. | JIADING Shanghai, China | Contract manufacturer, Contract sterilizer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Zhejiang Kindly Medical Devices Co., Ltd | WENZHOU Zhejiang, China | Contract manufacturer, Contract sterilizer | 0 | 0 | 0 | 0 | api.fda.gov | |
| ZHEJIANG LONGDE PHARMACEUTICAL Co., Ltd | HANGZHOU Zhejiang, China | Contract manufacturer, Contract sterilizer | 0 | 0 | 0 | 0 | api.fda.gov |
Updated February 19, 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.