Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3012499069

FEI Number

3012499069

Entity Name

CANFIELD SCIENTIFIC, INC.

City/State/Country

Parsippany, NJ, US

Establishment Address

4 Wood Hollow Road, Parsippany, NJ 07054, US

Establishment Type(s)

Manufacture Medical Device,Complaint File Establishment per 21 CFR 820.198

Owner / Operator

Canfield Scientific, Inc. (Owner Number: 10085027)

Owner / Operator Contact Address

4 Wood Hollow Road, Parsippany, NJ 07054, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

VEOS D2 Digital Dermatoscope VECTRA WB360 DermaGraphix IntelliStudio

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
KYT	Light, Examination, Medical, Battery Powered	General Hospital	Class 1	880.6350	2023-12-05
FTT	Camera, Still, Surgical	General, Plastic Surgery	Class 1	878.4160	2023-12-05

Official Correspondent

Douglas Canfield

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Canfield Scientific, 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 3012499069. Last updated year: 2026. Please use registration number 3012499069 when referencing this establishment in official correspondence.