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FDA 510(k)

Conometric Abutments

K-Number: K183079 · 2019-07-10

ApplicantDentsply Sirona, Inc.
Decision Date2019-07-10
Product CodeNHA
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

Conometric Abutments is the device name listed in this FDA 510(k) record. The listed applicant is Dentsply Sirona, Inc.. It received FDA 510(k) clearance on 2019-07-10 under 510(k) number K183079. The device is classified under product code NHA. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Conometric Abutments?

Conometric Abutments is a medical device that received FDA 510(k) clearance on 2019-07-10. The listed applicant is Dentsply Sirona, Inc.. The 510(k) number is K183079.

When did Conometric Abutments receive FDA 510(k) clearance?

Conometric Abutments received FDA 510(k) clearance on 2019-07-10, under 510(k) number K183079.

Who is the listed applicant for Conometric Abutments?

The FDA 510(k) record lists Dentsply Sirona, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Conometric Abutments?

The FDA product code for Conometric Abutments is NHA.

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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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