Data / Medical devices / Percutaneous Catheter, Ultrasound / United States
FDA-registered makers of Percutaneous Catheter, Ultrasound in the United States: 6 establishments
6 establishments in the United States are registered with the FDA to make Percutaneous Catheter, Ultrasound (product code PPN). 4 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
- Percutaneous Catheter, Ultrasound
- Product code
- PPN
- Country
- United States
Makers of Percutaneous Catheter, Ultrasound in the United States
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Shockwave Medical, Inc. | Santa Clara, CA, United States | Complaint file establishment, Manufacturer, Repackager or relabeler, Specification developer | 12 | July 27, 2026 | 0 | 1 | 0 | api.fda.gov |
| Bolt Medical Inc. | Carlsbad, CA, United States | Manufacturer, Specification developer | 2 | August 24, 2026 | 0 | 0 | 0 | api.fda.gov |
| Boston Scientific Corporation | Saint Paul, MN, United States | Complaint file establishment, Manufacturer | 2 | August 24, 2026 | 0 | 0 | 0 | api.fda.gov |
| Boston Scientific Corporation | Coventry, RI, United States | Manufacturer | 1 | March 25, 2025 | 0 | 0 | 0 | api.fda.gov |
| Onanon, Inc | Milpitas, CA, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Vanguard-Ems | Beaverton, OR, 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.