Data / Medical devices / Stimulator, Nerve, Peripheral, Electric / United States
FDA-registered makers of Stimulator, Nerve, Peripheral, Electric in the United States: 13 establishments
13 establishments in the United States are registered with the FDA to make Stimulator, Nerve, Peripheral, Electric (product code KOI). 4 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 2, 2026.
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- Device
- Stimulator, Nerve, Peripheral, Electric
- Product code
- KOI
- Country
- United States
Makers of Stimulator, Nerve, Peripheral, Electric 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 | 1 | December 5, 2016 | 0 | 0 | 0 | api.fda.gov |
| Blink Device Company | Seattle, WA, United States | Manufacturer | 1 | March 29, 2018 | 0 | 0 | 0 | api.fda.gov |
| Draeger Medical Systems, Inc. | Andover, MA, United States | Manufacturer | 1 | September 1, 2004 | 0 | 0 | 0 | api.fda.gov |
| Nerbio Medical Software Platforms, Inc. | San Jose, CA, United States | Specification developer | 1 | December 5, 2024 | 0 | 0 | 0 | api.fda.gov |
| Defibtech Branford | Branford, CT, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Ge Medical Systems Information Technologies | El Paso, TX, United States | Manufacturer, Repackager or relabeler | 0 | 0 | 0 | 0 | api.fda.gov | |
| GE Medical Systems Information Technologies, Inc. | Waukesha, WI, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| GE Medical Systems Information Technologies, Inc. | Wauwatosa, WI, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| MINDRAY DS USA, Inc. | Mahwah, NJ, United States | Complaint file establishment, 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 | |
| Philips North America LLC | Murrysville, PA, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Philips North America LLC | Export, PA, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Repair Operations Center | Oak Creek, WI, United States | Remanufacturer | 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.