Data / Medical devices / Wound Cleaner, Ultrasound / United States
FDA-registered makers of Wound Cleaner, Ultrasound in the United States: 6 establishments
6 establishments in the United States are registered with the FDA to make Wound Cleaner, Ultrasound (product code NRB). 3 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 3, 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
- Wound Cleaner, Ultrasound
- Product code
- NRB
- Country
- United States
Makers of Wound Cleaner, Ultrasound in the United States
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Arobella Medical, LLC | Minnetonka, MN, United States | Manufacturer | 2 | May 16, 2014 | 0 | 0 | 0 | api.fda.gov |
| Misonix, LLC | Farmingdale, NY, United States | Complaint file establishment, Manufacturer | 2 | March 5, 2013 | 0 | 0 | 0 | api.fda.gov |
| Sanuwave, Inc. | Eden Prairie, MN, United States | Manufacturer, Repackager or relabeler | 1 | August 13, 2014 | 0 | 0 | 0 | api.fda.gov |
| Donatelle Plastics, LLC | New Brighton, MN, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Dynamic Group | Ramsey, MN, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Nortech Systems, Inc. | Milaca, 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.