How Is HSB Classified?
Rod, Fixation, Intramedullary And Accessories is FDA product code HSB, Class 2, 21 CFR 888.3020.
What Does It Take to Sell It in the United States?
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. Chinese applicants hold 12 clearances under this code; the FDA took a median of 257 days from receipt to decision on them.
What Do the Recalls Say?
The FDA has recorded 690 recalls under this product code since 2003. None was by a company in China. The root causes the FDA records most often are Process change control (67), Employee error (67) and Process control (61).
A recall is a fact about one product and its maker, not a grade for every manufacturer of the type.