Medical Device Manufacturer · US , San Francisco , CA

Candesant Biomedical, Inc. - FDA 510(k) Cleared Devices

1 submissions · 0 cleared · Since 2023

1

Total

0

Cleared

1

Denied

Candesant Biomedical, Inc. has 0 FDA 510(k) cleared medical devices. Based in San Francisco, US.

Active since 2023. Primary specialty: General & Plastic Surgery.

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

FDA 510(k) cleared devices by Candesant Biomedical, Inc.

1 devices

1-1 of 1

Not Cleared Apr 07, 2023

The N-SWEAT Patch

DEN210055 · QVX

General & Plastic Surgery · 490d