MODULIGHT CORPORATION

FDA Device Registration & Listing · Tampere Pirkanmaa, FI · Registration 3006268530

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
3006268530
FEI Number
3006268530
Entity Name
MODULIGHT CORPORATION
City/State/Country
Tampere Pirkanmaa, FI
Establishment Address
Hermiankatu 22, Tampere Pirkanmaa 33720, FI
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Modulight Corporation (Owner Number: 10052625)
Owner / Operator Contact Address
Hermiankatu 22, Tampere, FI-11 33720, FI
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number

All Registered Proprietary Names

Photofrin 630 PDT laser ML7710-630-PIN ML7710 Modulight ML6710i Laser

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
MVF System, Laser, Photodynamic Therapy Unknown Class 3 N/A 2016-08-30
MVF System, Laser, Photodynamic Therapy Unknown Class 3 N/A 2023-05-11

Official Correspondent

Ancuta Guina

US Agent Details

Arthur S. Goddard Email: regulatory@modulight.com Phone: (216) 2335722

Related Public Records

Same Entity

Modulight Corporation
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 3006268530. Last updated year: 2026. Please use registration number 3006268530 when referencing this establishment in official correspondence.
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