Stryker Corporation - FDA 510(k) Cleared Devices

Stryker Corporation is an American multinational medical technology company headquartered in Portage, Michigan. The company develops and markets surgical equipment, neurotechnology, orthopedic implants, and patient safety systems used globally across medical specialties.

Stryker has received 81 FDA 510(k) clearances from 81 total submissions between 2010 and 2023. The company's cleared devices span orthopedic surgery, neurosurgery, general and plastic surgery, and ear, nose, and throat specialties. This regulatory record reflects the company's broad portfolio across surgical and neurotechnology domains.

Stryker's FDA 510(k) cleared devices include anterior cervical plating systems, ultrasonic aspirators, electromagnetic navigation instruments, and operating room information management platforms. The company's products are used by approximately 150 million patients annually across more than 75 countries, with significant market presence in orthopedic implants and neurosurgical technologies.

This profile represents Stryker's historical FDA 510(k) regulatory record. Explore the complete device clearance database to review specific product names, predicate devices, and clearance dates.