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Omnia Medical

2 FDA 510(k) clearances · Recalling firm

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RecordFirmDate
TiBrid Stand Alone Intervertebral Body Fusion Device, SA Angled Punch Awl, Sizes: 30 degre recall (Z-2556-2025)Omnia Medical2025-09-11
TiBrid Stand Alone Intervertebral Body Fusion Device, TiBrid SA Angled Screwdrivers, Sizes recall (Z-2557-2025)Omnia Medical2025-09-11

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Every clearance here is in the API, with alerts when new ones post.