Zimmer is one of 13027 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Zimmer - FDA 510(k) Cleared Devices
Recent clearances: Zimmer PSI Shoulder System, SMARTTOOLS KNEE SYSTEM
3
Total
3
Cleared
0
Denied
Zimmer, is a manufacturer specializing in orthopedic surgical devices and implants. The company operates with a manufacturing facility in Warsaw, US.
Zimmer has received 3 FDA 510(k) clearances from 3 total submissions. The company's regulatory history spans from 1984 to 2015, with all submissions focused on orthopedic devices. Notable cleared devices include the Zimmer PSI Shoulder System, SMARTTOOLS KNEE SYSTEM, and BIPOLAR HIP DEVICE. The company has been inactive in FDA submissions for more than five years and is maintained as a historical regulatory record.
Explore the complete list of device names, product codes, and clearance dates in the database.
FDA 510(k) Regulatory Record - Zimmer
3 devices