SOERING GMBH

FDA Device Registration & Listing · QUICKBORN Schleswig-Holstein, DE · Registration 9613895

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
9613895
FEI Number
3002808224
Entity Name
SOERING GMBH
City/State/Country
QUICKBORN Schleswig-Holstein, DE
Establishment Address
JUSTUS-VON-LIEBIG-RING 2, QUICKBORN Schleswig-Holstein D-25451, DE
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
SOERING GMBH (Owner Number: 9012241)
Owner / Operator Contact Address
Justus-von-Liebig-Ring 2, Quickborn, DE-SH 25451, DE
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
PMA Number
N/A

All Registered Proprietary Names

Sonoca-300 Sonoca 180/185 Wound Care System

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
BTA Pump, Portable, Aspiration (Manual Or Powered) General, Plastic Surgery Class 2 878.4780 2007-12-13
LFL Instrument, Ultrasonic Surgical Unknown Class U N/A 2007-12-13
LFL Instrument, Ultrasonic Surgical Unknown Class U N/A 2013-04-26

Official Correspondent

Inga Hauschildt

US Agent Details

Matt Kyle Business: Kuro Medical LLC Email: quality@kuromedical.com Phone: (612) 6362035

Related Public Records

Same Entity

SOERING GMBH
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0035-2007 Haemonetics Corporation 2
SmartSuction Harmony Powered Suction Device Model Number: HAR-E-115-US
Z-0332-2022 Covidien Llc U
Covidien Sonicision Battery Charger-intended to charge the Sonicision Reusable Battery Pack and to provide information on the battery charging progress and battery pack status Item Code: CBCA

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 9613895. Last updated year: 2026. Please use registration number 9613895 when referencing this establishment in official correspondence.
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