Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3042194079

FEI Number

3042194079

Entity Name

SWISS CUPPING AG

City/State/Country

Vaduz, LI

Establishment Address

Kirchstrasse 7, Vaduz 9490, LI

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Swiss Cupping AG (Owner Number: 10094379)

Owner / Operator Contact Address

Kirchstrasse 7, Vaduz, LI-11 9490, LI

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

PHALLOSAN forte PHALLOSAN vertical PHALLOSAN plus+

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
LKY	Device, External Penile Rigidity	Gastroenterology, Urology	Class 2	876.5020	2025-11-26

Official Correspondent

Julian Jochum

US Agent Details

Stefanie D. Bankston Email: vigilance@beoberlin.eu Phone: (713) 4834617

Related Public Records

Same Entity

Swiss Cupping AG

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 3042194079. Last updated year: 2026. Please use registration number 3042194079 when referencing this establishment in official correspondence.