ANTHROTRONIX, INC.

FDA Device Registration & Listing · Silver Spring, MD, US · Registration 3008375586

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
3008375586
FEI Number
3008375586
Entity Name
ANTHROTRONIX, INC.
City/State/Country
Silver Spring, MD, US
Establishment Address
8403 Colesville Rd Ste 1100, Silver Spring, MD 20910, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
AnthroTronix, Inc. (Owner Number: 10061127)
Owner / Operator Contact Address
8403 Colesville Road, Suite 1100, Silver Spring, MD 20910, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K141865
PMA Number
N/A

All Registered Proprietary Names

DANA

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
LQD Recorder, Attention Task Performance Unknown Class U N/A 2019-08-23

Official Correspondent

Lesley Siebenhausen

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

AnthroTronix, Inc.
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 3008375586. Last updated year: 2026. Please use registration number 3008375586 when referencing this establishment in official correspondence.
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