MT.DERM GmbH

FDA Device Registration & Listing · Berlin, DE · Registration 3006634874

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3006634874
FEI Number
3006634874
Entity Name
MT.DERM GmbH
City/State/Country
Berlin, DE
Establishment Address
Blohmstrasse 37-61, Berlin 12307, DE
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
MT.DERM GmbH (Owner Number: 10058532)
Owner / Operator Contact Address
Blohmstrasse 37 - 61, Berlin, DE-BE 12307, DE
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K182407
PMA Number
N/A

All Registered Proprietary Names

Footswitch 6-MNP 1.5 Exceed US 6-MNP 1.5 ToskaniMED US Bio Touch Precision Bio Touch Precision 6-MNP 1.5 Exceed US 6-MNP 1.5 ToskaniMED US Footswitch

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
QAI Powered Microneedle Device General, Plastic Surgery Class 2 878.4430 2018-10-08
QAI Powered Microneedle Device General, Plastic Surgery Class 2 878.4430 2019-07-22

Official Correspondent

Jan Tentrop

US Agent Details

David Burke Business: BioSkin Aesthetics Inc (BioSkin America Inc.) Email: dburke@bioskinaesthetics.com Phone: (561) 7041882

Related Public Records

Same Entity

MT.DERM GmbH
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 3006634874. Last updated year: 2026. Please use registration number 3006634874 when referencing this establishment in official correspondence.
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