Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

Ustomed Instrumente Ulrich Storz GmbH & Co. KG

FDA 510(k) & PMA Approved Devices — 1 products

Total Devices1
Categories1
Latest FDA decision2025-06-27
TypeNumberDevice NameCodeDateActions
510(k) K243190 USTOMED Bone Fixation/Bone Augmentation Systems - PINDZL2025-06-27 View