CROMA-PHARMA GMBH

FDA Device Registration & Listing · Leobendorf Niederosterreich, AT · Registration 3002806738

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
3002806738
FEI Number
3002806738
Entity Name
CROMA-PHARMA GMBH
City/State/Country
Leobendorf Niederosterreich, AT
Establishment Address
Industriezeile 6, Leobendorf Niederosterreich 2100, AT
Establishment Type(s)
Complaint File Establishment per 21 CFR 820.198,Manufacture Medical Device
Owner / Operator
CROMA-PHARMA GmbH (Owner Number: 10094137)
Owner / Operator Contact Address
Industriezeile 6, Leobendorf, AT-3 2100, AT
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number

All Registered Proprietary Names

saypha MagIQ

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 2025-11-17

Official Correspondent

Thomas Berger

US Agent Details

Natasha Hodkinson Business: Obagi Cosmeceuticals LLC Email: natasha.hodkinson@obagi.com Phone: (800) 6367546

Related Public Records

Same Entity

CROMA-PHARMA GmbH
View consolidated registration, premarket clearance, and recall records for this applicant.
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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3002806738. Last updated year: 2026. Please use registration number 3002806738 when referencing this establishment in official correspondence.
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