Data / Medical devices / Percussor, Powered-Electric / United States
FDA-registered makers of Percussor, Powered-Electric in the United States: 16 establishments
16 establishments in the United States are registered with the FDA to make Percussor, Powered-Electric (product code BYI). 12 have a 510(k) clearance or PMA approval on file and 1 has a recall event. FDA data exported November 2, 2026.
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- Device
- Percussor, Powered-Electric
- Product code
- BYI
- Country
- United States
Makers of Percussor, Powered-Electric in the United States
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Hill-Rom Manufacturing, Inc. | Saint Paul, MN, United States | Manufacturer, Repackager or relabeler | 4 | March 22, 2024 | 0 | 1 | 0 | api.fda.gov |
| Electromed, Inc. | New Prague, MN, United States | Complaint file establishment, Manufacturer | 3 | November 18, 2022 | 0 | 0 | 0 | api.fda.gov |
| Tactile Systems Technology Inc | New Brighton, MN, United States | Manufacturer | 2 | April 30, 2026 | 0 | 0 | 0 | api.fda.gov |
| Avanos Medical, Inc. | Alpharetta, GA, United States | Specification developer | 1 | February 20, 1986 | 0 | 0 | 0 | api.fda.gov |
| General Physiotherapy Ii LLC | Saint Charles, MO, United States | Manufacturer | 1 | January 23, 1986 | 0 | 0 | 0 | api.fda.gov |
| Icu Medical, Inc. | San Clemente, CA, United States | Complaint file establishment, Specification developer | 1 | August 18, 1981 | 0 | 0 | 0 | api.fda.gov |
| Intersurgical Inc. | Indianapolis, IN, United States | Manufacturer | 1 | October 23, 1991 | 0 | 0 | 0 | api.fda.gov |
| Med Systems | San Diego, CA, United States | Manufacturer | 1 | November 21, 2003 | 0 | 0 | 0 | api.fda.gov |
| Mercury Medical Enterprises, LLC | Clearwater, FL, United States | Manufacturer | 1 | November 22, 2013 | 0 | 0 | 0 | api.fda.gov |
| Respiratory Technologies, Inc. | Plymouth, MN, United States | Complaint file establishment, Specification developer | 1 | June 17, 2005 | 0 | 0 | 0 | api.fda.gov |
| SunMed Group Holdings, LLC | Grand Rapids, MI, United States | Complaint file establishment, Specification developer | 1 | February 20, 1986 | 0 | 0 | 0 | api.fda.gov |
| Thayer Medical Corportation | Tucson, AZ, United States | Manufacturer | 1 | August 6, 1998 | 0 | 0 | 0 | api.fda.gov |
| Core Products International Inc | Chetek, WI, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| ICU Medical, Inc. | Dublin, OH, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Multisource Manufacturing LLC | Longmont, CO, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Smooth-Bor Plastics | Laguna Hills, CA, 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.