NYF

Gingival Retraction Kit

Product code

NYF

Device name

Gingival Retraction Kit

Device class

Class 1

21 CFR

21 CFR 872.4565

Medical specialty

Dental

Marketing pathway

Enforcement Discretion

FDA classification definition

This product code has been established in accordance with the May 20, 1997, Guidance entitled, Convenience Kits Interim Regulatory Guidance, found at https://www.fda.gov/downloads/MedicalDevices/DeviceRegulationandGuidance/GuidanceDocuments/ucm080217.pdf. This type of convenience kit, as listed in the guidance above, is under enforcement discretion, and does not require a premarket notification (510(k)) to market if it meets all criteria in the guidance.

Definition text from the FDA device classification database (U.S. federal government work, public domain).