Zimmer Biomet - FDA 510(k) Cleared Devices

Zimmer Biomet, is a global leader in orthopedic innovations with a manufacturing facility in Warsaw, US. The company develops and markets surgical implants, instruments, and technologies for joint reconstruction and orthopedic care.

The company has received 5 FDA 510(k) clearances from 5 total submissions. All submissions focus on Orthopedic devices. The company's first clearance was in 2024, with the most recent in 2025, demonstrating active regulatory engagement.

Recent cleared devices include knee systems such as the Persona Partial Knee and Persona Personalized Knee System, hip reconstruction components including the Trabecular Metal Acetabular Revision System, and shoulder plating systems. The product portfolio reflects a core focus on joint arthroplasty and revision surgery solutions.

Explore the full list of device names, product codes, and clearance dates in the database.