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Nobel Biocare Dental Implant Systems Portfolio - MR Conditional

K212125 Class II Traditional
Decision Date
2021-09-24
Sponsor / Applicant
Nobel Biocare AG

Technical Specification

510(k) Submission ID K212125
Product Code DZE
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3640
Decision Date 2021-09-24
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Nobel Biocare Dental Implant Systems Portfolio - MR Conditional received FDA 510(k) clearance under submission number K212125, sponsored by Nobel Biocare AG. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2021-09-24.

Classification & Regulation

This clearance is catalogued under FDA product code DZE and 21 CFR 872.3640, within the Dental review panel as a Class II device.