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Dental devices

281 product codes reviewed by the Dental panel. 12,700 510(k) clearances and 1,349 recalls in the FDA data, 62% of those recalls name a 510(k).

222510(k)s in 12 months

32recalls in 12 months

832recalls that name a 510(k)

Active product codes, Class III

Code	Device	Class	510(k)s, 12 mo	Recalls, 12 mo
LZD	Joint, Temporomandibular, Implant	3	0	2
NQA	Biologic Material, Dental	3	0	1