Ustomed Instrumente Ulrich Storz GmbH & Co. KG is one of 234 FDA 510(k) medical device manufacturers from Germany in the dataset, ranked by real submission volume.
Ustomed Instrumente Ulrich Storz GmbH & Co. KG - FDA 510(k) Cleared D...
Recent clearances: USTOMED Bone Fixation/Bone Augmentation Systems - PIN
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Denied
Ustomed Instrumente Ulrich Storz GmbH & Co. KG has 1 FDA 510(k) cleared medical devices. Based in Tuttlingen, DE.
Latest FDA clearance: Jun 2025. Active since 2025. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Ustomed Instrumente Ulrich Storz GmbH & Co. KG Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Business Support International as regulatory consultant.
FDA 510(k) Regulatory Record - Ustomed Instrumente Ulrich Storz GmbH & Co. KG
1 devices