Lens, Contact (Other Material) – Daily

What Is FDA Product Code HQD?

Lens, Contact (Other Material) – Daily is FDA product code HQD, Class 2, 21 CFR 886.5916.

How Does It Reach the US Market?

A 510(k) premarket notification is required before it is sold in the United States: the applicant shows the device is substantially equivalent to one already on the market. The review can be done by an FDA-accredited third party, which is usually faster. Chinese applicants hold 2 clearances under this code; the FDA took a median of 139 days from receipt to decision on them.

What Do the Recalls Say?

The FDA has recorded 5 recalls under this product code since 2010. None was by a company in China. The root cause the FDA records most often is Process control (5).

A recall is a fact about one product and its maker, not a grade for every manufacturer of the type.