Medical Device Manufacturer · US , Somerset , NJ

Philips Lighting Co. - FDA 510(k) Cleared Devices

6 submissions · 6 cleared · Since 1991

Total

Cleared

Denied

Philips Lighting Co. has 6 FDA 510(k) cleared medical devices. Based in Somerset, US.

Historical record: 6 cleared submissions from 1991 to 2002. Primary specialty: General & Plastic Surgery.

Browse the FDA 510(k) cleared devices submitted by Philips Lighting Co. Filter by specialty or product code using the sidebar.

Philips Lighting Co. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Philips Lighting Co.

6 devices

1-6 of 6

Data Source

Sourced from the FDA 510(k) public files . 175,218 total devices indexed.

Last updated: Apr 27, 2026