Imex, LLC (manufacturer, Fulton, MD): 10 new FDA device listings, incl. electrode, cutaneous
Imex, LLC (Fulton, Maryland): 10 new FDA device listings, incl. electrode, cutaneous. Its amount of 10 is top-decile (93rd percentile of 2,570 records). Dated 182 days ago, it serves as a historical benchmark. Score 85/100. As of 2026-10-28, from openFDA device registration and listing endpoint (U.S. Food and Drug Administration).
Data as of · Compiled by Zalwin from openFDA device registration and listing endpoint (U.S. Food and Drug Administration)
amount: 10 · 93th percentile of 2,570 DeviceEstablishmentPulse records · 10.0x the median
Free preview: all 14 published fields of this record are shown below. Locked: 13 related MD DeviceEstablishmentPulse records and the 5-column CSV export.
| 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 |
| amount percentile | 93th of 2,570 (median 1, 10.0x median) |
| Peer records CSV (14 MD records) | 🔒 Click to unlock → |
| CRM-ready export with official source URLs | 🔒 Click to unlock → |
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CSV columns: Establishment · Role · New listings · Devices · Latest listing · official source URL
- Source agency: openFDA device registration and listing endpoint (U.S. Food and Drug Administration)
- Record date: 2026-05-06
- Data refreshed: 2026-10-28
- Refunds on request within 14 days
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LIVE PUBLIC DATA Source: openFDA device registration and listing endpoint (U.S. Food and Drug Administration) · Last refreshed: Wed, 28 Oct 2026 20:51:27 GMT
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Peer benchmark and outreach value: Imex, LLC and 14 Maryland peers
- Maryland DeviceEstablishmentPulse records like this one: 14
- Imex, LLC's amount: 93rd percentile of 2,570 records
- Timing: Low: older than 30 days
- Estimated pipeline if you contact every Maryland peer: $2,800 (peers × rate × deal size; an estimate from your assumptions, not a forecast)
85 / 100 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.
What is the DeviceEstablishmentPulse record for Imex, LLC in Fulton, Maryland?
Imex, LLC (Fulton, MD), a manufacturer, added 10 FDA device listings on 2026-05-06.
How does Imex, LLC compare to other Maryland DeviceEstablishmentPulse records?
This is a top-decile record: its amount of 10 is 10.0x the median of 1 across 2,570 records. It is 182 days old; check the official source for later updates before acting. Its Score of 85/100 puts it among the stronger signals in this feed.
Imex, LLC vs. top 3 peers
| Organization | Location | Amount | Percentile | Record date |
|---|---|---|---|---|
| Imex, LLC | Fulton, MD | 10 | 93rd | 2026-05-06 |
| Boston Scientific Corporation | Coventry, RI | 10 | 93rd | 2026-10-16 |
| Paragon 28 | Englewood, CO | 9 | 92nd | 2026-10-08 |
| Abyrx, Inc. | Stamford, CT | 7 | 90th | 2026-10-07 |
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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.