Dental Universal Implant Instrument Prosthetic Restoration Hand Driver Tools Kit

The sale of this item may be subject to regulation by the U. Food and Drug Administration and state and local regulatory agencies.

FDA for Curing Light: 510(K) Number: K192233, Regulation Number: 21 CFR 872.6070, Product Code: EBZ. FDA for Handpiece: 510(K) Number: K181691, Regulation Number: 872.4200, Classification Product Code: EFB, Subsequent Product Code: EGS. FDA for Scaler: 510(K) Number: K163414, Regulation Number: 872.4850, Product Code: ELC. IMPORTANT INFORMATION ON OUR POLICY AND FEEDBACK. Feedback if you are satisfied with our items.

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Please repack the item carefully.

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