360 AESTHETIC DEVICES, LLC

FDA Device Registration & Listing · Naples, FL, US · Registration 3023194151

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
3023194151
FEI Number
3023194151
Entity Name
360 AESTHETIC DEVICES, LLC
City/State/Country
Naples, FL, US
Establishment Address
5870 Washington St., Unit A, Naples, FL 34109, US
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
360 Aesthetic Devices, LLC (Owner Number: 10085474)
Owner / Operator Contact Address
5870 Washington St., Unit A, Naples, FL 34109, US
Initial Importer Flag
Y
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

NanoStamp 360 NanoStamp 360™

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
GFE Brush, Dermabrasion, Powered General, Plastic Surgery Class 1 878.4820 2022-06-22

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

360 Aesthetic Devices, LLC
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 3023194151. Last updated year: 2026. Please use registration number 3023194151 when referencing this establishment in official correspondence.
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