Flower Orthopedics Corporation DBA Conventus Flower Orthoped is one of 6918 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Flower Orthopedics Corporation DBA Conventus Flower Orthoped - FDA 51...
Recent clearances: OsteoCoil™ GT Active Compression System
1
Total
1
Cleared
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Denied
Flower Orthopedics Corporation DBA Conventus Flower Orthoped has 1 FDA 510(k) cleared medical devices. Based in Horsham, US.
Latest FDA clearance: Aug 2026. Active since 2026. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Flower Orthopedics Corporation DBA Conventus Flower Orthoped Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by DuVal & Associates, P.A. as regulatory consultant.
FDA 510(k) Regulatory Record - Flower Orthopedics Corporation DBA Conventus Flower Orthoped
1 devices