Philips Consumer Lifestyle B.V.

Philips Consumer Lifestyle B.V. — FDA 510(k) Submissions

Philips Consumer Lifestyle B.V. has submitted 2 FDA 510(k) premarket notifications since 2025, of which 2 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Light Based Over-the-counter Hair Removal . Use the specialty filter in the sidebar to narrow results.