EASEMED

FDA Device Registration & Listing · Ashburn, VA, US · Registration 3032857683

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
3032857683
FEI Number
3032857683
Entity Name
EASEMED
City/State/Country
Ashburn, VA, US
Establishment Address
44679 Endicott Dr Ste 300, Pmb 836, Ashburn, VA 20147, US
Establishment Type(s)
Complaint File Establishment per 21 CFR 820.198,Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
EaseMed LLC (Owner Number: 10091479)
Owner / Operator Contact Address
44679 Endicott Drive, Ste 300 #836, Ashburn, VA 20147, US
Initial Importer Flag
Y
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

NOZECALM

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
NAB Gauze / Sponge,Nonresorbable For External Use General, Plastic Surgery Class 1 878.4014 2024-10-07

Official Correspondent

Neel Vekaria

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

EaseMed LLC
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 3032857683. Last updated year: 2026. Please use registration number 3032857683 when referencing this establishment in official correspondence.
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