FDA applicant
Soring GmbH Medizintechnik
FDA records 7 decisions for Soring GmbH Medizintechnik (Denton, TX) from 1999 to 2010: 7 510(k) clearances. Most are in product codes GEI (Electrosurgical, Cutting & Coagulation &…) and LFL (Instrument, Ultrasonic Surgical). Its devices cite 8 predicates, 5 of them its own earlier devices. No recall is linked to its devices.
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly
How often FDA has decided Soring GmbH Medizintechnik’s devices, and how often a recall has named them.
FDA decisions per year
1in 2010
2026 so far, outlined.
Recalls per year
No recall linked to its devices since 2007.
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