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FDA 510(k)

NOBELREPLACE TAPERED CONICAL CONNECTION

K-Number: K062566 · 2006-12-06

Decision Date2006-12-06
Product CodeDZE
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

NOBELREPLACE TAPERED CONICAL CONNECTION is the device name listed in this FDA 510(k) record. The listed applicant is Nobel Biocare USA, LLC. It received FDA 510(k) clearance on 2006-12-06 under 510(k) number K062566. 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 NOBELREPLACE TAPERED CONICAL CONNECTION?

NOBELREPLACE TAPERED CONICAL CONNECTION is a medical device that received FDA 510(k) clearance on 2006-12-06. The listed applicant is Nobel Biocare USA, LLC. The 510(k) number is K062566.

When did NOBELREPLACE TAPERED CONICAL CONNECTION receive FDA 510(k) clearance?

NOBELREPLACE TAPERED CONICAL CONNECTION received FDA 510(k) clearance on 2006-12-06, under 510(k) number K062566.

Who is the listed applicant for NOBELREPLACE TAPERED CONICAL CONNECTION?

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

What is the FDA product code for NOBELREPLACE TAPERED CONICAL CONNECTION?

The FDA product code for NOBELREPLACE TAPERED CONICAL CONNECTION 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.

Other records listing Nobel Biocare USA, LLC 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.

View all 7 devices →

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.

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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