Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3017254114

FEI Number

3017254114

Entity Name

DERMASENSOR INC

City/State/Country

Miami, FL, US

Establishment Address

801 Brickell Ave Ste 1610, Miami, FL 33131, US

Establishment Type(s)

Complaint File Establishment per 21 CFR 820.198,Develop Specifications But Do Not Manufacture At This Facility

Owner / Operator

DermaSensor Inc (Owner Number: 10090725)

Owner / Operator Contact Address

801 Brickell Ave, # 1610, Miami, FL 33131, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

DEN230008

PMA Number

N/A

All Registered Proprietary Names

DermaSensor

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
QZS	Software-Aided Adjunctive Diagnostic Device For Use By Physicians On Lesions Suspicious For Skin Cancer	General, Plastic Surgery	Class 2	878.1830	2024-05-22

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

DermaSensor 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 3017254114. Last updated year: 2026. Please use registration number 3017254114 when referencing this establishment in official correspondence.