Groups of medical devices drawn from live regulatory data, showing which regulators each device is registered with.
Every device we hold with a US FDA 510(k) clearance decided in the last 12 months, newest first. Each one links through to its full regulatory record.
Devices the FDA identifies as using artificial intelligence or machine learning, with the regulators each one is registered with.
Devices the FDA identifies as using augmented or virtual reality, with the regulators each one is registered with.
Devices the FDA identifies as sensor-based, with the regulators each one is registered with.