Data / Medical devices / Saline, Vascular Access Flush / United States
FDA-registered makers of Saline, Vascular Access Flush in the United States: 12 establishments
12 establishments in the United States are registered with the FDA to make Saline, Vascular Access Flush (product code NGT). 9 have a 510(k) clearance or PMA approval on file and 5 have a recall event. FDA data exported November 2, 2026.
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- Device
- Saline, Vascular Access Flush
- Product code
- NGT
- Country
- United States
Makers of Saline, Vascular Access Flush in the United States
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Becton Dickinson | Franklin Lakes, NJ, United States | Specification developer | 5 | December 2, 2025 | 0 | 4 | 0 | api.fda.gov |
| Medefil, Inc. | Glendale Heights, IL, United States | Contract manufacturer, Manufacturer, Repackager or relabeler | 4 | September 20, 2012 | 0 | 0 | 0 | api.fda.gov |
| Aquabiliti | Nashville, TN, United States | Complaint file establishment, Contract manufacturer, Manufacturer | 3 | August 13, 2014 | 0 | 5 | 0 | api.fda.gov |
| Excelsior Medical LLC | Neptune, NJ, United States | Manufacturer | 3 | September 15, 2019 | 0 | 3 | 0 | api.fda.gov |
| Becton Dickinson And Company | Columbus, NE, United States | Manufacturer | 2 | February 2, 2017 | 0 | 0 | 0 | api.fda.gov |
| Nurse Assist, LLC | Haltom City, TX, United States | Manufacturer | 2 | August 11, 2020 | 0 | 2 | 2 | api.fda.gov |
| Excelsior Medical LLC | Tinton Falls, NJ, United States | Manufacturer | 1 | June 21, 2018 | 0 | 0 | 0 | api.fda.gov |
| Medline Industries, LP - ReadyCare Hartland | Hartland, WI, United States | Manufacturer | 1 | June 21, 2018 | 0 | 0 | 0 | api.fda.gov |
| Spectra Medical Devices, LLC | Wilmington, MA, United States | Specification developer | 1 | July 29, 2011 | 0 | 1 | 1 | api.fda.gov |
| Bound Tree Medical, LLC | Grand Prairie, TX, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| CLAYENS Crystal Lake, LLC | Crystal Lake, IL, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Piccolo Medical | San Francisco, CA, United States | Complaint file establishment, Manufacturer, Repackager or relabeler, Specification developer | 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.