# Imex, LLC (manufacturer, Fulton, MD): 10 new FDA device listings, incl. electrode, cutaneous

**Score:** 85/100

| Field | Value |
|---|---|
| Establishment | Imex, LLC |
| Role | Manufacturer |
| Establishment types | Manufacture Medical Device; Develop Specifications But Do Not Manufacture At This Facility |
| Location | Fulton, MD, US |
| New listings | 10 |
| Devices | Electrode, Cutaneous; Pack, Hot Or Cold, Water Circulating; Lamp, Infrared, Therapeutic Heating; Stimulator, Nerve, Transcutaneous, For Pain Relief; Interferential Current Therapy; Ultrasonic Diathermy For Use In Applying Therapeutic Deep Heat; Stimulator, Muscle, Powered; Pack, Hot Or Cold, Reusable |
| Product codes | GXY, ILO, ILY, GZJ, LIH, IMI, IPF, IME |
| Device classes | Class I, Class II |
| Medical specialties | Neurology, Physical Medicine |
| Brand names | Dynatron ThermoStim TM Probe DTSP1; Dynatron Solaris Plus Ultrasound Probe WSH05; Dynatron Plus 625; Dynatron Solaris Plus 709; Dynatron Plus 925; Dynatron Solaris Plus 706; Dynatron Tri-Wave Light Probe DCP3; Dynatron Tri-Wave Light Pad DLP3 |
| First new listing | 2026-05-06 |
| Latest new listing | 2026-05-06 |
| FDA registration number | 3030151584 |
| Registration expires | 2026-12-31 |

## Why this score
- Brings its own devices to market: buys manufacturing, sterilization and QMS help.
- Class II or III devices: QMS and regulatory demands.
- Several new listings at once.
- U.S. establishment.

Source: openFDA device registration and listing endpoint (U.S. Food and Drug Administration) (https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm). Last refreshed: 2026-10-28T20:51:27.468Z.
From the openFDA device registration and listing data, refreshed weekly. A listing shows a device an establishment says it makes or handles for the U.S. market; it is not FDA clearance or approval. Contact persons and street addresses are not stored. Verify in the FDA Establishment Registration and Device Listing database.