Data / Medical devices / Electromagnetic Stimulator, Pain Relief
Electromagnetic Stimulator, Pain Relief (QPL): 6 FDA-registered makers in 6 countries
6 establishments in 6 countries are registered with the FDA to make Electromagnetic Stimulator, Pain Relief (product code QPL, Class 2, 21 CFR 882.5890). 5 of them have a 510(k) clearance or PMA approval on file and 0 have a recall event. The FDA has issued 6 510(k) clearances under this code, the latest on August 7, 2025, and lists 0 recall events (0 Class I). FDA data exported November 2, 2026.
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- Product code
- QPL
- Device class
- 2
- Regulation
- 882.5890
- Medical specialty
- Neurology
Makers by country
| Country | Makers |
|---|---|
| United States | 1 |
| Bulgaria | 1 |
| Slovenia | 1 |
| United Kingdom | 1 |
| Denmark | 1 |
| Czechia | 1 |
Makers of Electromagnetic Stimulator, Pain Relief
Registered establishments that manufacture, contract manufacture, remanufacture, reprocess or own the specification of this device, with the 510(k) clearances, PMA approvals and recalls the FDA files under each. Best documented first.
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Neuralace Medical | San Marcos, CA, United States | Complaint file establishment, Specification developer | 2 | January 10, 2024 | 0 | 0 | 0 | api.fda.gov |
| BTL Industries JSC | Plovdiv, Bulgaria | Manufacturer | 1 | August 7, 2025 | 0 | 0 | 0 | api.fda.gov |
| Fotona D.O.O. | Ljubljana, Slovenia | Manufacturer | 1 | March 27, 2025 | 0 | 0 | 0 | api.fda.gov |
| The Magstim Company Ltd. | Carmarthenshire Wales, United Kingdom | Manufacturer | 1 | July 3, 2025 | 0 | 0 | 0 | api.fda.gov |
| Tonica Elektronik A/S | FARUM Hovedstaden, Denmark | Manufacturer | 1 | August 25, 2023 | 0 | 0 | 0 | api.fda.gov |
| Deymed Diagnostic S.R.O. | Hronov Nachod, Czechia | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov |
Updated August 7, 2025. 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.