Data / Medical devices / Flowmeter, Blood, Cardiovascular / United States
FDA-registered makers of Flowmeter, Blood, Cardiovascular in the United States: 14 establishments
14 establishments in the United States are registered with the FDA to make Flowmeter, Blood, Cardiovascular (product code DPW). 10 have a 510(k) clearance or PMA approval on file and 3 have a recall event. FDA data exported November 2, 2026.
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- Device
- Flowmeter, Blood, Cardiovascular
- Product code
- DPW
- Country
- United States
Makers of Flowmeter, Blood, Cardiovascular in the United States
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Remington Medical, Inc. | Alpharetta, GA, United States | Manufacturer | 3 | November 20, 2025 | 0 | 0 | 0 | api.fda.gov |
| Remington Medical, Inc. | Alpharetta, GA, United States | Manufacturer | 3 | November 20, 2025 | 0 | 0 | 0 | api.fda.gov |
| Transonic Systems, Inc. | Ithaca, NY, United States | Manufacturer | 2 | December 21, 2011 | 0 | 1 | 0 | api.fda.gov |
| Coopersurgical, Inc. | Trumbull, CT, United States | Manufacturer, Specification developer | 1 | March 16, 2011 | 0 | 0 | 0 | api.fda.gov |
| Cook Incorporated | Bloomington, IN, United States | Complaint file establishment, Manufacturer | 1 | March 16, 2011 | 0 | 0 | 0 | api.fda.gov |
| Hemedex Incorporated | North Waltham, MA, United States | Manufacturer | 1 | May 8, 2002 | 0 | 0 | 0 | api.fda.gov |
| SYNOVIS MICRO COMPANIES ALLIANCE, INC. (a subsidiary of Baxter International Inc.) | Birmingham, AL, United States | Manufacturer, Specification developer | 1 | October 28, 2008 | 0 | 0 | 0 | api.fda.gov |
| Terumo Cardiovascular Systems Corporation | Elkton, MD, United States | Manufacturer | 1 | May 14, 2003 | 0 | 0 | 0 | api.fda.gov |
| Vascular Technology Incorporated | Nashua, NH, United States | Manufacturer | 1 | October 28, 2008 | 0 | 2 | 0 | api.fda.gov |
| ev3, Inc. | Plymouth, MN, United States | Specification developer | 1 | January 10, 2020 | 0 | 0 | 0 | api.fda.gov |
| Cook Incorporated | Ellettsville, IN, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Parks Medical Electronics, Inc. | Aloha, OR, United States | Manufacturer | 0 | 0 | 2 | 0 | api.fda.gov | |
| Spartronics Strongsville, Inc. | Strongsville, OH, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Spectrum Plastics Group | Saint Louis Park, MN, United States | Contract 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.