Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3041244757

FEI Number

3041244757

Entity Name

ARTAFLEX BUFFALO INC.

City/State/Country

Buffalo, NY, US

Establishment Address

550 Colvin Avenue, Buffalo, NY 14216, US

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer)

Owner / Operator

Artaflex Buffalo Inc. (Owner Number: 10094032)

Owner / Operator Contact Address

550 Colvin Avenue, Buffalo, NY 14216, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

MolecuLightDX+

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
QJF	Autofluorescence Imaging Adjunct Tool For Wounds	General, Plastic Surgery	Class 2	878.4550	2025-11-17

Official Correspondent

Jorge Mar

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Artaflex Buffalo Inc.

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

Similar Registrations

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3013443304	EXACT MEDICAL MANUFACTURING, INC.	Changzhou Jiangsu, CN
3039395626	ADIUVO DIAGNOSTICS PRIVATE LIMITED	Visakhapatnam Andhra Pradesh, IN
3001744314	SWIFT MEDICAL	Toronto Ontario, CA
3014704068	MOLECULIGHT INC.	TORONTO Ontario, CA
3018781093	EXACT MEDICAL MANUFACTURING, INC.	Changzhou Jiangsu, CN

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3041244757. Last updated year: 2026. Please use registration number 3041244757 when referencing this establishment in official correspondence.