Data / Medical devices / Catheter, Conduction, Anesthetic / United States
FDA-registered makers of Catheter, Conduction, Anesthetic in the United States: 13 establishments
13 establishments in the United States are registered with the FDA to make Catheter, Conduction, Anesthetic (product code BSO). 12 have a 510(k) clearance or PMA approval on file and 5 have a recall event. FDA data exported November 3, 2026.
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- Device
- Catheter, Conduction, Anesthetic
- Product code
- BSO
- Country
- United States
Makers of Catheter, Conduction, Anesthetic in the United States
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Avanos Medical, Inc. | Alpharetta, GA, United States | Complaint file establishment, Specification developer | 7 | September 30, 2016 | 0 | 1 | 0 | api.fda.gov |
| Epimed International, Inc. | Johnstown, NY, United States | Complaint file establishment, Contract manufacturer, Manufacturer | 5 | April 27, 2020 | 0 | 2 | 0 | api.fda.gov |
| B. Braun Medical Inc. | Bethlehem, PA, United States | Specification developer | 3 | September 15, 2023 | 0 | 0 | 0 | api.fda.gov |
| Icu Medical, Inc. | San Clemente, CA, United States | Complaint file establishment, Specification developer | 3 | October 18, 2006 | 0 | 0 | 0 | api.fda.gov |
| Axiom Medical, Inc. | Torrance, CA, United States | Manufacturer | 2 | May 17, 2000 | 0 | 0 | 0 | api.fda.gov |
| Arrow International LLC (subsidiary of Teleflex Incorporated) | Morrisville, NC, United States | Specification developer | 2 | March 17, 2017 | 0 | 2 | 1 | api.fda.gov |
| Arrow International, LLC (subsidiary of Teleflex Incorporated) | Wyomissing, PA, United States | Specification developer | 2 | March 17, 2017 | 0 | 3 | 0 | api.fda.gov |
| B. Braun Us Device Manufacturing LLC | Allentown, PA, United States | Contract manufacturer, Repackager or relabeler | 2 | June 29, 2009 | 0 | 1 | 0 | api.fda.gov |
| MEDLINE INDUSTRIES, LP - Northfield | Northfield, IL, United States | Specification developer | 2 | March 4, 2019 | 0 | 0 | 0 | api.fda.gov |
| BD Puerto Rico LLC | Juncos, PR, United States | Manufacturer | 1 | March 11, 1985 | 0 | 0 | 0 | api.fda.gov |
| Becton Dickinson | Franklin Lakes, NJ, United States | Specification developer | 1 | March 11, 1985 | 0 | 0 | 0 | api.fda.gov |
| Spinal Elements, Inc. | Carlsbad, CA, United States | Complaint file establishment, Manufacturer | 1 | January 19, 2011 | 0 | 0 | 0 | api.fda.gov |
| Vascular Solutions LLC | Maple Grove, MN, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov |
Updated November 3, 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.