Medical Device Manufacturer · US , Champaign , IL

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

2 submissions · 2 cleared · Since 2019

Total

Cleared

Denied

Photonicare, Inc. has 2 FDA 510(k) cleared medical devices. Based in Champaign, US.

Last cleared in 2022. Active since 2019. Primary specialty: Ear, Nose, Throat.

Browse the FDA 510(k) cleared devices submitted by Photonicare, Inc. Filter by specialty or product code using the sidebar.

Photonicare, Inc. 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 - Photonicare, Inc.

2 devices

1-2 of 2