Data / Medical devices / Heparin, Vascular Access Flush
Heparin, Vascular Access Flush (NZW): 4 FDA-registered makers in 1 country
4 establishments in 1 country are registered with the FDA to make Heparin, Vascular Access Flush (product code NZW, Class 2, 21 CFR 880.5200). 4 of them have a 510(k) clearance or PMA approval on file and 2 have a recall event. The FDA has issued 7 510(k) clearances under this code, the latest on February 27, 2017, and lists 11 recall events (0 Class I). FDA data exported November 2, 2026.
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- Product code
- NZW
- Device class
- 2
- Regulation
- 880.5200
- Medical specialty
- General Hospital
Makers by country
| Country | Makers |
|---|---|
| United States | 4 |
Makers of Heparin, Vascular Access Flush
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 |
|---|---|---|---|---|---|---|---|---|
| Becton Dickinson | Franklin Lakes, NJ, United States | Manufacturer, Specification developer | 2 | February 27, 2017 | 0 | 0 | 0 | api.fda.gov |
| Becton Dickinson And Company | Columbus, NE, United States | Manufacturer | 2 | February 27, 2017 | 0 | 0 | 0 | api.fda.gov |
| Excelsior Medical LLC | Neptune, NJ, United States | Manufacturer | 1 | November 14, 2014 | 0 | 2 | 0 | api.fda.gov |
| Medefil, Inc. | Glendale Heights, IL, United States | Contract manufacturer, Manufacturer | 1 | February 3, 2010 | 0 | 3 | 0 | api.fda.gov |
Updated February 27, 2017. 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.