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FDA 510(k)

Nobel Biocare Dental Implant Systems Portfolio - MR Conditional

K-Number: K212125 · 2021-09-24

ApplicantNobel Biocare AG
Decision Date2021-09-24
Product CodeDZE
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

Nobel Biocare Dental Implant Systems Portfolio - MR Conditional is the device name listed in this FDA 510(k) record. The listed applicant is Nobel Biocare AG. It received FDA 510(k) clearance on 2021-09-24 under 510(k) 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. The listed applicant is Nobel Biocare AG. The 510(k) number is K212125.

When did Nobel Biocare Dental Implant Systems Portfolio - MR Conditional receive FDA 510(k) clearance?

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

Who is the listed applicant for Nobel Biocare Dental Implant Systems Portfolio - MR Conditional?

The FDA 510(k) record lists Nobel Biocare AG as the applicant. This does not by itself establish the device manufacturer.

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.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

NCT06086873Investigating Implant Surface Effect on Osseointegration: NGA vs. ModSLARECRUITINGNCT07280260Clinical Performance of Nobel N1 SystemRECRUITING

Other records listing Nobel Biocare AG as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K200040Universal Base Conical Connection (CC)

Related Devices (Code: DZE)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K251188UNIQA® Dental Implants SystemUniqa Dental, Ltd.K251232MegaGen Zygoma Dental Implant SystemMegagen Implant Co., Ltd.K250806Dental Implant SystemA.B. Dental Devices , Ltd.K260006INOSS SystemInosys, Inc.K252731Promimic ZrP Surface Dental Implant; Promimic ZrP + HAnano Surface Dental ImplantPromimic ABK252031Adin Long Dental Implant SystemAdin Dental Implant Systems , Ltd.

Official Source

View on FDA Database →

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

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