Yes. Tampons are regulated by FDA as Class II medical devices, and sanitary pads may also be subject to FDA oversight as medical devices. Importers should ensure products meet FDA labeling and premarket notification requirements and be prepared for FDA examination at the port of entry.

Heading 9619 is explicitly material-neutral — products qualify regardless of whether they are made from textile, nonwoven, polymer film, or composite materials. Classification is driven by the article's function as an absorbent personal hygiene product rather than by its constituent fiber or material.