Takara Belmont Corporation is one of 18423 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Takara Belmont Corporation - FDA 510(k) Cleared Devices
Recent clearances: Bel-Cypher Pro, Evogue Dental Unit, PHOT-X IIS MODEL 505
4
Total
4
Cleared
0
Denied
Takara Belmont Corporation has 4 FDA 510(k) cleared medical devices. Based in Somerset, US.
Historical record: 4 cleared submissions from 2011 to 2017. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Takara Belmont Corporation Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Schiff & Company, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Takara Belmont Corporation
4 devices