Data / Medical devices / Stimulator, Spinal-Cord, Implanted (Pain Relief) / United States
FDA-registered makers of Stimulator, Spinal-Cord, Implanted (Pain Relief) in the United States: 19 establishments
19 establishments in the United States are registered with the FDA to make Stimulator, Spinal-Cord, Implanted (Pain Relief) (product code GZB). 9 have a 510(k) clearance or PMA approval on file and 3 have a recall event. FDA data exported November 2, 2026.
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- Device
- Stimulator, Spinal-Cord, Implanted (Pain Relief)
- Product code
- GZB
- Country
- United States
Makers of Stimulator, Spinal-Cord, Implanted (Pain Relief) in the United States
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Abbott Medical | Plano, TX, United States | Manufacturer | 11 | May 2, 2014 | 0 | 2 | 0 | api.fda.gov |
| Curonix LLC | Pompano Beach, FL, United States | Complaint file establishment, Manufacturer, Specification developer | 9 | November 7, 2019 | 0 | 0 | 0 | api.fda.gov |
| Medtronic Neuromodulation | Minneapolis, MN, United States | Manufacturer | 7 | October 26, 2010 | 0 | 2 | 0 | api.fda.gov |
| Medtronic Puerto Rico Operations Co., Villalba | Villalba, PR, United States | Manufacturer | 3 | August 16, 2006 | 0 | 0 | 0 | api.fda.gov |
| Boston Scientific Neuromodulation Corporation | Valencia, CA, United States | Complaint file establishment, Specification developer | 2 | August 23, 2024 | 0 | 1 | 0 | api.fda.gov |
| Medtronic Puerto Rico Operations Co., Juncos | Juncos, PR, United States | Manufacturer | 2 | October 26, 2010 | 0 | 0 | 0 | api.fda.gov |
| Abbott Medical | Arecibo, PR, United States | Manufacturer | 1 | May 22, 1996 | 0 | 0 | 0 | api.fda.gov |
| Boston Scientific Corporation | Saint Paul, MN, United States | Manufacturer | 1 | February 23, 2012 | 0 | 0 | 0 | api.fda.gov |
| Nalu Medical | Carlsbad, CA, United States | Manufacturer, Specification developer | 1 | August 23, 2024 | 0 | 0 | 0 | api.fda.gov |
| Cirtec Medical | Enfield, CT, United States | Contract manufacturer, Contract sterilizer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Heraeus Medical Components, LLC | Saint Paul, MN, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Life Science Outsourcing, Inc. | Brea, CA, United States | Contract manufacturer, Contract sterilizer | 0 | 0 | 0 | 0 | api.fda.gov | |
| MiniStim Corp | Boca Raton, FL, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Oscor Inc. | Palm Harbor, FL, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Pro-Tech Design & MFG., Inc. | Santa Fe Springs, CA, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| PRO-TECH Design & Mfg, Inc. | Santa Fe Springs, CA, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| PRO-TECH Design & Mfg, Inc. | Arlington, TX, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Spectrum Assembly Inc. | Carlsbad, CA, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Technical Services For Electronics, Inc. | Jackson, 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.