Aromha, Inc

FDA Device Registration & Listing · Potomac, MD, US · Registration 3042838444

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
3042838444
FEI Number
3042838444
Entity Name
Aromha, Inc
City/State/Country
Potomac, MD, US
Establishment Address
10008 Hemswell Ln, Potomac, MD 20854, US
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility,Manufacture Medical Device
Owner / Operator
Aromha Inc (Owner Number: 10094807)
Owner / Operator Contact Address
10008 Hemswell Ln, Potomac, MD 20854, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Aromha Brain Health Test

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
NRK Kit, Test, Olfactory Ear, Nose, Throat Class 2 874.1600 2025-12-24

Official Correspondent

Sean Reineke

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Aromha Inc
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 3042838444. Last updated year: 2026. Please use registration number 3042838444 when referencing this establishment in official correspondence.
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