Respire Medical Holding is one of 18408 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Respire Medical Holding - FDA 510(k) Cleared Devices
Recent clearances: Respire Pink Series with DentiTrac, Respire Blue Series-EF, Respire Pink Series-Herbst-EF
3
Total
3
Cleared
0
Denied
Respire Medical Holding has 3 FDA 510(k) cleared medical devices. Based in Brooklyn, US.
Historical record: 3 cleared submissions from 2015 to 2017. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Respire Medical Holding Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Quality Solutions and Support, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Respire Medical Holding
3 devices