Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3031562618

FEI Number

3031562618

Entity Name

Aliform B.V.

City/State/Country

Maastricht Limburg, NL

Establishment Address

Oxfordlaan 55, Maastricht Limburg 6229 EV, NL

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Aliform B.V. (Owner Number: 10090974)

Owner / Operator Contact Address

Oxfordlaan 55, Maastricht, NL-LI 6229EV, NL

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Celluleaf

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
GDI	Dissector, Surgical, General & Plastic Surgery	General, Plastic Surgery	Class 1	878.4800	2024-06-10

Official Correspondent

Victor Suturin

US Agent Details

Edwin Lindsay Business: RAF SOLUTIONS USA, INC Email: edwin@rafsolutions.net Phone: (305) 9607262

Related Public Records

Same Entity

Aliform B.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 3031562618. Last updated year: 2026. Please use registration number 3031562618 when referencing this establishment in official correspondence.