Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3018101388

FEI Number

3018101388

Entity Name

MICUTEC AG

City/State/Country

Zug, CH

Establishment Address

Chamerstrasse 172, Zug 6300, CH

Establishment Type(s)

Develop Specifications But Do Not Manufacture At This Facility

Owner / Operator

miCUTec AG (Owner Number: 10080844)

Owner / Operator Contact Address

Chamerstrasse 172, Zug, CH-ZG 6300, CH

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

No proprietary names listed under this establishment.

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
HAB	Saw, Powered, And Accessories	General, Plastic Surgery	Class 1	878.4820	2021-03-02

Official Correspondent

No official correspondent registered.

US Agent Details

Angelika Scherp Email: info@bsi-fda.com Phone: (212) 3318358

Related Public Records

Same Entity

miCUTec 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 3018101388. Last updated year: 2026. Please use registration number 3018101388 when referencing this establishment in official correspondence.