Data / Medical devices / Catheter, Straight / United States
FDA-registered makers of Catheter, Straight in the United States: 11 establishments
11 establishments in the United States are registered with the FDA to make Catheter, Straight (product code EZD). 11 have a 510(k) clearance or PMA approval on file and 1 has a recall event. FDA data exported November 2, 2026.
SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.
- Device
- Catheter, Straight
- Product code
- EZD
- Country
- United States
Makers of Catheter, Straight in the United States
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| HR PHARMACEUTICALS, INC d/b/a HR HealthCare | York, PA, United States | Complaint file establishment, Specification developer | 4 | June 24, 2026 | 0 | 0 | 0 | api.fda.gov |
| Hollister Incorporated | Libertyville, IL, United States | Specification developer | 3 | May 18, 2026 | 0 | 0 | 0 | api.fda.gov |
| C.R. Bard, Inc. | Covington, GA, United States | Specification developer | 2 | September 20, 2017 | 0 | 2 | 0 | api.fda.gov |
| Compactcath, Inc | Palo Alto, CA, United States | Specification developer | 2 | June 14, 2018 | 0 | 0 | 0 | api.fda.gov |
| Greystone Medical, LLC | Waterford, MI, United States | Specification developer | 2 | October 28, 2014 | 0 | 0 | 0 | api.fda.gov |
| MEDLINE INDUSTRIES, LP - Northfield | Northfield, IL, United States | Specification developer | 2 | February 22, 2018 | 0 | 0 | 0 | api.fda.gov |
| Adapta Medical, Inc. | Colorado Springs, CO, United States | Complaint file establishment, Manufacturer | 1 | August 16, 2016 | 0 | 0 | 0 | api.fda.gov |
| Avanos Medical, Inc. | Alpharetta, GA, United States | Complaint file establishment, Specification developer | 1 | December 19, 2007 | 0 | 0 | 0 | api.fda.gov |
| Cardinal Health | Hazelwood, MO, United States | Specification developer | 1 | November 7, 1997 | 0 | 0 | 0 | api.fda.gov |
| Footprint Medical Inc. | San Antonio, TX, United States | Manufacturer | 1 | August 12, 2009 | 0 | 0 | 0 | api.fda.gov |
| Icu Medical, Inc | Salt Lake City, UT, United States | Specification developer | 1 | May 13, 2008 | 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.