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Bio-C Repair Ion+

K201222 Class II Traditional
Decision Date
2021-02-11
Sponsor / Applicant
Angelus Industria DE Produtos Odontologicos S/A

Technical Specification

510(k) Submission ID K201222
Product Code KIF
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3820
Decision Date 2021-02-11
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Bio-C Repair Ion+ received FDA 510(k) clearance under submission number K201222, sponsored by Angelus Industria DE Produtos Odontologicos S/A. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2021-02-11.

Classification & Regulation

This clearance is catalogued under FDA product code KIF and 21 CFR 872.3820, within the Dental review panel as a Class II device.