Stryker Endoscopy - FDA 510(k) Cleared Devices

Stryker Endoscopy, is a medical device manufacturer based in San Jose, US. The company specializes in endoscopic and surgical imaging systems for minimally invasive procedures.

Stryker Endoscopy has received 102 FDA 510(k) clearances from 103 total submissions since its first clearance in 1993. The company maintains active regulatory status, with its latest clearance in 2026. Its portfolio spans General & Plastic Surgery devices, orthopedic surgical tools, and obstetric and gynecologic instruments.

Recent cleared devices include advanced imaging systems such as 4K camera platforms, LED light sources with advanced imaging modality, and connected operating room hubs with integrated device and voice control. The company also manufactures specialized surgical instruments including laparoscopes, cystoscopes, hysteroscopes, and biocomposite anchors for orthopedic applications.

Explore the complete list of device names, product codes, and clearance dates in the database to review Stryker Endoscopy's full regulatory history.

Regulatory submissions have been managed by Underwriters Laboratories, Inc., Third Party Review Group, LLC and Tuv Rheinland of North America, Inc..