Remover, Intrauterine Device, Contraceptive, Hook-Type

What Is FDA Product Code HHF?

Remover, Intrauterine Device, Contraceptive, Hook-Type is FDA product code HHF, Class 1, 21 CFR 884.4530.

What Does It Take to Sell It in the United States?

It is exempt from premarket notification: the manufacturer registers its establishment and lists the device, and no 510(k) is needed before it is sold in the United States.

What Has Gone Wrong With It?

The FDA has recorded 1 recall under this product code since 2024. None was by a company in China. A recall is a fact about one product and its maker, not a grade for every manufacturer of the type.