Stryker Corp. - FDA 510(k) Cleared Devices

Stryker Corp. is an American multinational medical technology company headquartered in Portage, Michigan. The company develops and markets surgical equipment, implants, and patient safety technologies used globally across multiple medical specialties.

Stryker has received 121 FDA 510(k) clearances from 124 total submissions since its first clearance in 1976. The company maintains active regulatory engagement, with its latest clearance in 2023. Its product portfolio spans orthopedic devices, neurosurgical implants, surgical instruments, and endoscopy systems, reflecting a broad presence across surgical and neurotechnology markets.

Recent cleared devices include spinal systems, joint replacement implants, arthroscopy equipment, and specialized surgical attachments and guides. These products serve orthopedic surgery, neurology, radiology, and general surgical applications. Stryker's devices are used by approximately 150 million patients annually across more than 75 countries, underscoring the company's scale and clinical reach.

Explore the complete regulatory record by reviewing individual device names, product codes, and FDA 510(k) clearance dates in the database.