ARCERA GMBH

FDA Device Registration & Listing · Munich Bavaria, DE · Registration 3015373820

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
3015373820
FEI Number
3015373820
Entity Name
ARCERA GMBH
City/State/Country
Munich Bavaria, DE
Establishment Address
Levelingstrasse 8, Munich Bavaria 81673, DE
Establishment Type(s)
Repack or Relabel Medical Device
Owner / Operator
Arcera GmbH (Owner Number: 10060255)
Owner / Operator Contact Address
Levelingstrasse 8, Munich, DE-BY 81673, DE
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
P170007

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
LMH Implant, Dermal, For Aesthetic Use Unknown Class 3 N/A 2019-07-26
MOZ Acid, Hyaluronic, Intraarticular Unknown Class 3 N/A 2019-04-16
LMH Implant, Dermal, For Aesthetic Use Unknown Class 3 N/A 2019-07-26
MOZ Acid, Hyaluronic, Intraarticular Unknown Class 3 N/A 2019-04-16
LMH Implant, Dermal, For Aesthetic Use Unknown Class 3 N/A 2019-07-26
LMH Implant, Dermal, For Aesthetic Use Unknown Class 3 N/A 2019-07-26
PKY Implant, Dermal, For Aesthetic Use In The Hands Unknown Class 3 N/A 2019-07-26
LMH Implant, Dermal, For Aesthetic Use Unknown Class 3 N/A 2019-07-26
MOZ Acid, Hyaluronic, Intraarticular Unknown Class 3 N/A 2019-04-16
PKY Implant, Dermal, For Aesthetic Use In The Hands Unknown Class 3 N/A 2019-07-28
LMH Implant, Dermal, For Aesthetic Use Unknown Class 3 N/A 2019-07-28
MOZ Acid, Hyaluronic, Intraarticular Unknown Class 3 N/A 2019-10-30

Official Correspondent

Franz-Josef Wienhold

US Agent Details

FDAIMPORTS.COM LLC Email: registration@fdaimports.com Phone: (410) 2202800

Related Public Records

Same Entity

Arcera 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 3015373820. Last updated year: 2026. Please use registration number 3015373820 when referencing this establishment in official correspondence.
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