Thermidas Americas, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Thermidas Americas, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Thermidas IR System (ThIR-A615)
1
Total
1
Cleared
0
Denied
Thermidas Americas, Inc. has 1 FDA 510(k) cleared medical devices. Based in South Pasadena, US.
Last cleared in 2021. Active since 2021. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Thermidas Americas, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Gunster, Yoakley & Stewart, P.A. as regulatory consultant.
FDA 510(k) Regulatory Record - Thermidas Americas, Inc.
1 devices