Data / Medical devices / Electrode, Depth / United States
FDA-registered makers of Electrode, Depth in the United States: 9 establishments
9 establishments in the United States are registered with the FDA to make Electrode, Depth (product code GZL). 6 have a 510(k) clearance or PMA approval on file and 2 have a recall event. FDA data exported November 2, 2026.
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- Device
- Electrode, Depth
- Product code
- GZL
- Country
- United States
Makers of Electrode, Depth in the United States
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Ad-Tech Medical Instrument Corp. | Oak Creek, WI, United States | Manufacturer | 6 | May 18, 2023 | 0 | 5 | 0 | api.fda.gov |
| PMT Corp. | Chanhassen, MN, United States | Contract manufacturer, Manufacturer, Repackager or relabeler, Specification developer | 5 | July 14, 2016 | 0 | 0 | 0 | api.fda.gov |
| Blackrock Microsystems | Salt Lake City, UT, United States | Manufacturer | 3 | February 9, 2011 | 0 | 0 | 0 | api.fda.gov |
| FHC, Inc. | Bowdoin, ME, United States | Manufacturer | 3 | December 20, 2018 | 0 | 3 | 0 | api.fda.gov |
| Neuroone Medical Technologies Corp. | Eden Prairie, MN, United States | Complaint file establishment, Specification developer | 2 | October 20, 2022 | 0 | 0 | 0 | api.fda.gov |
| FISHER WALLACE LABORATORIES Inc | Brooklyn, NY, United States | Specification developer | 1 | September 7, 1990 | 0 | 0 | 0 | api.fda.gov |
| Cirtec Medical | Brooklyn Park, MN, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| LISI MEDICAL Remmele | Coon Rapids, MN, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Qxmedical, LLC | Saint Paul, MN, 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.