Sequon, LLC

FDA Device Registration & Listing · Annapolis, MD, US · Registration 3011581939

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
3011581939
FEI Number
3011581939
Entity Name
Sequon, LLC
City/State/Country
Annapolis, MD, US
Establishment Address
601 Chinquapin Round Road, Annapolis, MD 21401, US
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
Sequon, LLC (Owner Number: 10049104)
Owner / Operator Contact Address
601 Chinquapin Round Road, Annapolis, MD 21401, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Medherent Medherent

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
NXQ Reminder, Medication Physical Medicine Class 1 890.5050 2015-04-15
NXB Dispenser, Solid Medication Physical Medicine Class 1 890.5050 2015-04-14

Official Correspondent

Yeardley Green

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Sequon, LLC
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K944481 Garan Scientific, Inc. THE HEART PROTECTOR 1995-04-10

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3011581939. Last updated year: 2026. Please use registration number 3011581939 when referencing this establishment in official correspondence.
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