Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3004538228

FEI Number

3004538228

Entity Name

FIRST LINE TECHNOLOGY

City/State/Country

Fredericksburg, VA, US

Establishment Address

487 Lendall Lane, Fredericksburg, VA 22405, US

Establishment Type(s)

Repack or Relabel Medical Device,Manufacture Medical Device

Owner / Operator

First Line Technology (Owner Number: 10031973)

Owner / Operator Contact Address

487 Lendall Lane, Fredericksburg, VA 22405, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

FiberTect Wipe FiberTect Pad FiberTect Mitt

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
FRL	Fiber, Medical, Absorbent	General Hospital	Class 1	880.5300	2026-06-12

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

First Line Technology

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3004538228. Last updated year: 2026. Please use registration number 3004538228 when referencing this establishment in official correspondence.