LUMENXT, LLC

FDA Device Registration & Listing · Knoxville, TN, US · Registration 3017482216

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3017482216
FEI Number
3017482216
Entity Name
LUMENXT, LLC
City/State/Country
Knoxville, TN, US
Establishment Address
3665 Iskagna Dr, Knoxville, TN 37919, US
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
LumeNXT, LLC (Owner Number: 10093119)
Owner / Operator Contact Address
3665 Iskagna Dr, Knoxville, TN 37919, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

No proprietary names listed under this establishment.

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
FTG Illuminator, Remote General, Plastic Surgery Class 2 878.4580 2025-04-01

Official Correspondent

Chris Doody

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

LumeNXT, LLC
View consolidated registration, premarket clearance, and recall records for this applicant.
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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3017482216. Last updated year: 2026. Please use registration number 3017482216 when referencing this establishment in official correspondence.
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