Data / Medical devices / Electrode, Electrosurgical / United States
FDA-registered makers of Electrode, Electrosurgical in the United States: 13 establishments
13 establishments in the United States are registered with the FDA to make Electrode, Electrosurgical (product code JOS). 4 have a 510(k) clearance or PMA approval on file and 1 has a recall event. FDA data exported November 3, 2026.
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- Device
- Electrode, Electrosurgical
- Product code
- JOS
- Country
- United States
Makers of Electrode, Electrosurgical in the United States
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Linvatec Corporation | Largo, FL, United States | Manufacturer | 2 | August 20, 1999 | 0 | 0 | 0 | api.fda.gov |
| Gyrus ACMI, Inc. | Brooklyn Park, MN, United States | Manufacturer | 1 | May 16, 1995 | 0 | 0 | 0 | api.fda.gov |
| Kirwan Surgical Products, LLC. | Marshfield, MA, United States | Manufacturer | 1 | September 15, 1989 | 0 | 0 | 0 | api.fda.gov |
| Megadyne Medical Products, Inc. | Cincinnati, OH, United States | Specification developer | 1 | October 2, 1990 | 0 | 0 | 0 | api.fda.gov |
| Conmed Corporation | Utica, NY, United States | Complaint file establishment, Manufacturer | 0 | 0 | 1 | 0 | api.fda.gov | |
| Cynosure, LLC | Westford, MA, United States | Complaint file establishment, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| ConMed Corporation | Greenwood Village, CO, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Covidien | Plainfield, IN, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Covidien | Boulder, CO, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Covidien | Lafayette, CO, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Custom Manufacturing Inc. | Elbert, CO, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| New Deantronics, Ltd. | Sparks, NV, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Paragon Medical - Mansfield, Bridgemedica | Mansfield, MA, 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.