Stryker - FDA 510(k) Cleared Devices

Stryker is a family of eight-wheeled armored fighting vehicles derived from the Canadian LAV III. The vehicles are produced by General Dynamics Land Systems-Canada for the United States Army in London, Ontario.

This historical record documents 92 FDA 510(k) cleared devices from 92 total submissions between 2006 and 2023. The company's regulatory portfolio focused primarily on General & Plastic Surgery devices, including advanced imaging systems, LED light sources, and surgical visualization equipment. The company has been inactive, with no clearances recorded in more than five years.

Notable cleared device categories include 4K camera systems with advanced imaging modality, LED light sources with integrated illumination technology, laparoscopic visualization tools, and orthopedic implant systems. These devices supported general surgery, plastic surgery, and orthopedic applications.

Explore the complete regulatory history by reviewing individual device names, product codes, and clearance dates in the database.