Soering G M B H

FDA Filings

This page includes the latest FDA filings for Soering G M B H. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.

FDA Registration(s)
Registration Number9613895
FEI Number3002808224
NameSOERING GMBH
Owner & OperatorSOERING GMBH
Contact AddressJustus-von-Liebig-Ring 2
Quickborn DE-SH Schleswig-Holstein 25451 DE
Official Correspondent
  • Insa Endrweit
  • 49-4106-61000-215
US Agent
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration AddressJUSTUS-VON-LIEBIG-RING 2
QUICKBORN Schleswig-Holstein, D-25451 DE
Establishment Type
  • Manufacture Medical Device
  • Manufacture Medical Device for Another Party (Contract Manufacturer)

Registration Number3010973847
FEI Number3010973847
NameSoring, Inc.
Owner & OperatorSoering GmbH
Contact AddressJustus-von-Liebig-Ring 2
Quickborn DE-SH Schleswig-Holstein 25451 DE
Registration Status1
Initial ImporterY
Registration Expiration2020-04-25
Registration Address7771 W Oakland Park Blvd Ste 221
Sunrise, FL 33351 US

FDA Filings

Device
Company
DeviceDate
SOERING GMBH
Sonoca 180/185 Wound Care System2013-04-26
SOERING GMBH
Aquamantys Pump Generator 230V2012-11-22
SOERING GMBH
Aquamantys Pump Generator 115V2012-11-22
SOERING GMBH
40-403-1 (230 Volt)2012-11-22
SOERING GMBH
40-402-1 (115 Volt)2012-11-22
SOERING GMBH
SONOCA 180/195 WOUND CARE SYSTEM2008-05-21
SOERING GMBH
Sonoca-3002007-12-13
SOERING GMBH
Sonoca-3002007-12-13
SOERING GMBH
Sonoca-1902007-12-13
SOERING GMBH
Sonoca-1802007-12-13

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