Church & Dwight Co., Inc.

Church & Dwight Co., Inc. — FDA 510(k) Submissions

Church & Dwight Co., Inc. has submitted 29 FDA 510(k) premarket notifications since 2006, of which 29 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Condom, Lubricant, Personal, Condom, Synthetic, Kit, Test, Pregnancy, Hcg, Over The Counter, Lubricant, Personal, Gamete, Fertilization, And Embryo Compatible . Use the specialty filter in the sidebar to narrow results.