Pfizer, Inc. - FDA 510(k) Cleared Devices

Pfizer, Inc. is an American multinational pharmaceutical and biotechnology corporation headquartered in Manhattan, New York City. Founded in 1849, Pfizer is one of the oldest pharmaceutical companies in North America.

Pfizer's FDA 510(k) regulatory record includes 30 cleared devices from 30 total submissions, spanning 1977 to 2018. The company's device portfolio demonstrates strength in orthopedic devices, including surgical implants and fixation systems. This regulatory activity is now historical, with no clearances recorded in the past five years.

The company's cleared device categories span multiple specialties, including orthopedic implants, neurology devices, ophthalmic products, dental instruments, wound care, and gastroenterology tools. Notable cleared devices include orthopedic components such as hip bolts, femoral bolts, and acetabular components, alongside therapeutic and diagnostic devices across other medical disciplines.

Explore the complete record of device names, product codes, and clearance dates in the database below.