Data / Medical devices / Transducer, Pressure, Catheter Tip / United States
FDA-registered makers of Transducer, Pressure, Catheter Tip in the United States: 16 establishments
16 establishments in the United States are registered with the FDA to make Transducer, Pressure, Catheter Tip (product code DXO). 10 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 2, 2026.
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- Device
- Transducer, Pressure, Catheter Tip
- Product code
- DXO
- Country
- United States
Makers of Transducer, Pressure, Catheter Tip in the United States
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Becton, Dickinson And Company | Irvine, CA, United States | Specification developer | 6 | December 22, 2022 | 0 | 0 | 0 | api.fda.gov |
| St. Jude Medical, Cardiology Division, Inc. | Plymouth, MN, United States | Specification developer | 4 | March 28, 2018 | 0 | 0 | 0 | api.fda.gov |
| Millar LLC. | Houston, TX, United States | Manufacturer | 3 | March 10, 2017 | 0 | 0 | 0 | api.fda.gov |
| Acist Medical Systems, Inc. | Eden Prairie, MN, United States | Manufacturer | 2 | July 17, 2024 | 0 | 0 | 0 | api.fda.gov |
| Abbott Medical | Westford, MA, United States | Specification developer | 1 | March 28, 2018 | 0 | 0 | 0 | api.fda.gov |
| Boston Scientific Corporation | Maple Grove, MN, United States | Manufacturer | 1 | December 23, 2019 | 0 | 0 | 0 | api.fda.gov |
| Boston Scientific Corporation | Coventry, RI, United States | Manufacturer | 1 | December 23, 2019 | 0 | 0 | 0 | api.fda.gov |
| Edwards Lifesciences Technology Sarl | Anasco, PR, United States | Manufacturer | 1 | September 3, 2014 | 0 | 0 | 0 | api.fda.gov |
| St. Jude Medical, Atrial Fibrillation Division, Inc. | Saint Paul, MN, United States | Manufacturer | 1 | March 2, 2012 | 0 | 0 | 0 | api.fda.gov |
| Zurich Medical Inc | Plymouth, MN, United States | Manufacturer | 1 | August 14, 2019 | 0 | 0 | 0 | api.fda.gov |
| EPIC MedTec OEM Catheter & Wire LLC | Plymouth, MN, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Freudenberg Medical, LLC | Jeffersonville, IN, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Metal Craft Machine & Engineering, Inc. | Elk River, MN, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Riverside Machine & Engineering, Inc. | Eau Claire, WI, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Volcano Corporation | Rancho Cordova, CA, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Volcano Corporation | San Diego, CA, United States | Complaint file establishment, 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.