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FDA 510(k)

NOBELACTIVE INTERNAL CONNECTION IMPLANT

K-Number: K071370 · 2007-08-03

ApplicantNobel Biocare AB
Decision Date2007-08-03
Product CodeDZE
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

NOBELACTIVE INTERNAL CONNECTION IMPLANT is the device name listed in this FDA 510(k) record. The listed applicant is Nobel Biocare AB. It received FDA 510(k) clearance on 2007-08-03 under 510(k) number K071370. 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 NOBELACTIVE INTERNAL CONNECTION IMPLANT?

NOBELACTIVE INTERNAL CONNECTION IMPLANT is a medical device that received FDA 510(k) clearance on 2007-08-03. The listed applicant is Nobel Biocare AB. The 510(k) number is K071370.

When did NOBELACTIVE INTERNAL CONNECTION IMPLANT receive FDA 510(k) clearance?

NOBELACTIVE INTERNAL CONNECTION IMPLANT received FDA 510(k) clearance on 2007-08-03, under 510(k) number K071370.

Who is the listed applicant for NOBELACTIVE INTERNAL CONNECTION IMPLANT?

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

What is the FDA product code for NOBELACTIVE INTERNAL CONNECTION IMPLANT?

The FDA product code for NOBELACTIVE INTERNAL CONNECTION IMPLANT is DZE.

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Other records listing Nobel Biocare AB as applicant

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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.

K261392TriActive Dental Implant SystemParagon Implant Mfg., LLCK260463ZEROS Dental Implant SystemZeros Co., Ltd.K251188UNIQA® Dental Implants SystemUniqa Dental, Ltd.K251232MegaGen Zygoma Dental Implant SystemMegagen Implant Co., Ltd.K250806Dental Implant SystemA.B. Dental Devices , Ltd.K260006INOSS SystemInosys, Inc.

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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