Data / Medical devices / Germany / Soering GMBH
Soering GMBH: FDA-registered device maker in QUICKBORN Schleswig-Holstein, Germany, 2 510(k) clearances
Soering GMBH is registered with the FDA (registration 9613895) in QUICKBORN Schleswig-Holstein, Germany. It lists 2 device types. The FDA files 2 510(k) clearances under its listings, the newest dated May 21, 2008. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 9613895
- FEI number
- 3002808224
- Address
- Justus-Von-Liebig-Ring 2, QUICKBORN Schleswig-Holstein, Germany, D-25451
- Owner or operator
- SOERING GMBH (9012241)
- Roles
- Manufacturer
- First device listed
- December 13, 2007
- Registered through
- 2026
- Brand names listed
- Sonoca 180/185 Wound Care System, Sonoca-300
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Instrument, Ultrasonic Surgical | LFL | U | Manufacturer | accessdata.fda.gov |
| Pump, Portable, Aspiration (Manual Or Powered) | BTA | 2 | Manufacturer | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| May 21, 2008 | K072904 | SONOCA 180/195 WOUND CARE SYSTEM | LFL | Substantially Equivalent | Soering GmbH | accessdata.fda.gov |
| September 23, 1999 | K992026 | SORING GMBH, SONOCA 300 | BTA | Substantially Equivalent | Soring GmbH Medizintechnik | accessdata.fda.gov |
Compare with other makers
- All makers of Pump, Portable, Aspiration (Manual Or Powered)
- All makers of Instrument, Ultrasonic Surgical
Updated May 21, 2008. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.