Stryker Sustainability Solutions is one of 12953 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Stryker Sustainability Solutions - FDA 510(k) Cleared Devices
Recent clearances: Remanufactured LigaSure XP Maryland Jaw Sealer/Divider Without Nano-coating, Reprocessed HARMONIC 700 Shears (HAR723/Reprocessed HARMONIC 700, 5mm Diameter Shears with Advanced Hemostasis x 23cm), Reprocessed RD SET Adt Pulse Oximeter Sensor (4000)
Stryker Sustainability Solutions has 32 FDA 510(k) cleared medical devices. Based in Tempe, US.
Latest FDA clearance: Jun 2026. Active since 2011. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Stryker Sustainability Solutions Filter by specialty or product code using the sidebar.
1 device has linked clinical trial registered on ClinicalTrials.gov. 1 submission has an FDA-authorized Predetermined Change Control Plan (PCCP), indicating AI or software-based device development.