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Data / Medical devices / United States / First Line Technology

First Line Technology: FDA-registered device maker in Fredericksburg, VA, United States, 1 510(k) clearance

First Line Technology is registered with the FDA (registration 3004538228) in Fredericksburg, VA, United States. It lists 2 device types. The FDA files 1 510(k) clearance under its listings, the newest dated April 22, 2003. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number
3004538228
Address
487 Lendall Lane, Fredericksburg, VA, United States, 22405
Owner or operator
First Line Technology (10031973)
Roles
Manufacturer, Repackager or relabeler
First device listed
May 7, 2025
Registered through
2026
Brand names listed
BabyPod 2, BabyPod 20, FiberTect Mitt, FiberTect Pad, FiberTect Wipe, NeoPod

Devices it lists

DeviceProduct codeClassRoleSource
Fiber, Medical, AbsorbentFRL1Manufacturer, Repackager or relabeleraccessdata.fda.gov
Stretcher, Hand-CarriedFPP1Repackager or relabeleraccessdata.fda.gov

510(k) clearances

The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.

Decided510(k) numberDeviceProduct codeDecisionApplicantSource
April 22, 2003K030283BABY PODFPPSubstantially EquivalentPrism Enterprises, Inc.accessdata.fda.gov

Compare with other makers

Updated April 22, 2003. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.