Trumedx LLC (other, Shelton, CT): 5 new FDA device listings, incl. lamp, infrared, therapeutic heating
Trumedx LLC (Shelton, Connecticut): 5 new FDA device listings, incl. lamp, infrared, therapeutic heating. Its amount of 5 is above the median of 1 (87th percentile). Dated 158 days ago, it serves as a historical benchmark. Score 65/100. 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: 5 · 87th percentile of 2,570 DeviceEstablishmentPulse records · 5.0x the median
Free preview: all 15 published fields of this record are shown below. Locked: 13 related CT DeviceEstablishmentPulse records and the 5-column CSV export.
| Field | Value |
|---|---|
| Establishment | Trumedx LLC |
| Owner / operator | TrumedX LLC |
| Role | Other |
| Establishment types | Complaint File Establishment per 21 CFR 820.198 |
| Location | Shelton, CT, US |
| New listings | 5 |
| Devices | Lamp, Infrared, Therapeutic Heating; Massager, Powered Inflatable Tube; Sleeve, Limb, Compressible; Pack, Hot Or Cold, Water Circulating |
| Product codes | ILY, IRP, JOW, ILO |
| Device classes | Class II |
| Medical specialties | Physical Medicine, Cardiovascular |
| Brand names | TruLuminate; TruMedX Wraps; Bighorn Ice |
| First new listing | 2026-05-12 |
| Latest new listing | 2026-05-30 |
| FDA registration number | 3032062344 |
| Registration expires | 2026-12-31 |
| amount percentile | 87th of 2,570 (median 1, 5.0x median) |
| Peer records CSV (14 CT 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: 2026-05-30
- Data refreshed: 2026-10-28
- Refunds on request within 14 days
Top DeviceEstablishmentPulse records (CT first): TOMZ Corporation (contract manufacturer, Berlin, CT) · Coopersurgical, Inc. (manufacturer, Trumbull, CT) · Abyrx, Inc. (manufacturer, Stamford, CT) · Linemaster Switch Corp. (contract manufacturer, Woodstock, C · Spine Wave, Inc. (manufacturer, Shelton, CT) · Browse all by state and category →
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: Trumedx LLC and 14 Connecticut peers
- Connecticut DeviceEstablishmentPulse records like this one: 14
- Trumedx LLC's amount: 87th percentile of 2,570 records
- Timing: Low: older than 30 days
- Estimated pipeline if you contact every Connecticut peer: $2,800 (peers × rate × deal size; an estimate from your assumptions, not a forecast)
65 / 100 Score
- Class II or III devices: QMS and regulatory demands.
- Several new listings at once.
- U.S. establishment.
What is the DeviceEstablishmentPulse record for Trumedx LLC in Shelton, Connecticut?
Trumedx LLC (Shelton, CT), a other, added 5 FDA device listings between 2026-05-12 and 2026-05-30.
How does Trumedx LLC compare to other Connecticut DeviceEstablishmentPulse records?
Its amount of 5 sits in the upper half (87th percentile) of 2,570 records; the median is 1. It is 158 days old; check the official source for later updates before acting.
Trumedx LLC vs. top 3 peers
| Organization | Location | Amount | Percentile | Record date |
|---|---|---|---|---|
| Trumedx LLC | Shelton, CT | 5 | 87th | 2026-05-30 |
| Merz North America, Inc. | Sturtevant, WI | 4 | 83rd | 2026-09-23 |
| Rapid Medical Inc. | Southlake, TX | 4 | 83rd | 2026-09-20 |
| Metier Medical (USA) LLC | Ponte Vedra Beach, FL | 7 | 90th | 2026-10-16 |
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DeviceEstablishmentPulse: Other DeviceEstablishmentPulse: U.S. establishment DeviceEstablishmentPulse: records in Connecticut
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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.