Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3019769561

FEI Number

3019769561

Entity Name

ScarPro NV

City/State/Country

Aalter Flanders, BE

Establishment Address

Lobulckstraat 3, Aalter Flanders 9880, BE

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Scarpro N.V. (Owner Number: 10082066)

Owner / Operator Contact Address

Lobulckstraat 3, Aalter, BE-NOTA 9880, BE

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Mederma Silicone Scar Sheet

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
MDA	Elastomer, Silicone, For Scar Management	General, Plastic Surgery	Class 1	878.4025	2021-06-11

Official Correspondent

Christel Van Wonterghem

US Agent Details

Steven Weisman Business: Lumanity Email: Steven.weisman@lumanity.com Phone: (973) 8161130

Related Public Records

Same Entity

Scarpro N.V.

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 3019769561. Last updated year: 2026. Please use registration number 3019769561 when referencing this establishment in official correspondence.