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FDA 510(k)

Nobel Biocare Dental Implant Systems Portfolio - MR Conditional

K-Number: K212125 · 2021-09-24

Decision Date2021-09-24
Product CodeDZE
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

Nobel Biocare Dental Implant Systems Portfolio - MR Conditional is a medical device manufactured by Nobel Biocare AG. It received FDA 510(k) clearance on 2021-09-24 under approval number K212125. The device is classified under product code DZE. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Nobel Biocare Dental Implant Systems Portfolio - MR Conditional?

Nobel Biocare Dental Implant Systems Portfolio - MR Conditional is a medical device that received FDA 510(k) clearance on 2021-09-24. It is manufactured by Nobel Biocare AG. The 510(k) number is K212125.

When was Nobel Biocare Dental Implant Systems Portfolio - MR Conditional approved by the FDA?

Nobel Biocare Dental Implant Systems Portfolio - MR Conditional received FDA 510(k) clearance on 2021-09-24, under approval number K212125.

What company makes Nobel Biocare Dental Implant Systems Portfolio - MR Conditional?

Nobel Biocare Dental Implant Systems Portfolio - MR Conditional is manufactured by Nobel Biocare AG.

What is the FDA product code for Nobel Biocare Dental Implant Systems Portfolio - MR Conditional?

The FDA product code for Nobel Biocare Dental Implant Systems Portfolio - MR Conditional is DZE.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.