Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3029906593

FEI Number

3029906593

Entity Name

Super Seton B.V.

City/State/Country

Amsterdam Noord-Holland, NL

Establishment Address

Paasheuvelweg 25, Amsterdam Noord-Holland 1105 BP, NL

Establishment Type(s)

Develop Specifications But Do Not Manufacture At This Facility

Owner / Operator

Super Seton B.V. (Owner Number: 10088670)

Owner / Operator Contact Address

Paasheuvelweg 25, Amsterdam, NL-NOTA 1105 BP, NL

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

SuperSeton

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
GBN	Catheter, Pediatric, General & Plastic Surgery	General, Plastic Surgery	Class 1	878.4200	2023-10-03

Official Correspondent

No official correspondent registered.

US Agent Details

Matthew Dryden Business: ProMedic, LLC Email: matt.dryden@promedic.cc Phone: (239) 3076063

Related Public Records

Same Entity

Super Seton 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 3029906593. Last updated year: 2026. Please use registration number 3029906593 when referencing this establishment in official correspondence.