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FDA 510(k)

CAPO BULK FILL

K-Number: K152471 · 2016-08-04

ApplicantSchuetz Dental GmbH
Decision Date2016-08-04
Product CodeEBF
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

CAPO BULK FILL is a medical device manufactured by Schuetz Dental GmbH. It received FDA 510(k) clearance on 2016-08-04 under approval number K152471. The device is classified under product code EBF. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CAPO BULK FILL?

CAPO BULK FILL is a medical device that received FDA 510(k) clearance on 2016-08-04. It is manufactured by Schuetz Dental GmbH. The 510(k) number is K152471.

When was CAPO BULK FILL approved by the FDA?

CAPO BULK FILL received FDA 510(k) clearance on 2016-08-04, under approval number K152471.

What company makes CAPO BULK FILL?

CAPO BULK FILL is manufactured by Schuetz Dental GmbH.

What is the FDA product code for CAPO BULK FILL?

The FDA product code for CAPO BULK FILL is EBF.

Related Devices (Code: EBF)

K163207Filtek One Bulk Fill Restorative3M Company K162537CAD/CAMouflage Milling BlockPrismatik Dentalcraft, Inc. K160049CharismaHeraeus Kulzer, LLC (Mitsui Chemicals Group) K162257P1145 Dental RestorativeKerr Corporation K151399Capo Hybrid, Capo Slow Flow, Capo Flow, Capo Natural, Capo Universal, Nano Paq, Nano Paq FlowSchutz Dental GmbH K162107TPH Spectra+ Universal Composite RestorativeDentsply Sirona

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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