Soering GmbH
Country not established FDA
- Devices
- 1
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA establishment
What Soering GmbH makes
Soering GmbH makes wound care systems, such as the SONOCA 180/195 WOUND CARE SYSTEM.
The company's portfolio is regulated under device class U and is listed in the FDA 510k registry, with the company based in the US.
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Sonoca 180/195 Wound Care System Ref K072904
Regimes: 510(k) Registry: 510(k)
FDA establishments
- Soering GmbH QUICKBORN Schleswig-Holstein · DE FEI 3002808224
Frequently asked questions
How many devices does Soering GmbH have in the registry?
The registry currently lists 1 device for Soering GmbH. Devices recorded under merged duplicate company entries are counted once.
Which registries list Soering GmbH's devices?
Among its 1 most recently registered device, Soering GmbH has devices listed in FDA 510(k) (1 device).
What are the newest devices from Soering GmbH in the registry?
The most recently registered devices listed for Soering GmbH include SONOCA 180/195 WOUND CARE SYSTEM.
Which FDA establishments are linked to Soering GmbH?
1 FDA establishment is linked to Soering GmbH in the registry; they are listed on the company page.