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FDA 510(k)

Nobilplast Denture Resin

K-Number: K170375 · 2017-10-02

ApplicantCmp Industries, LLC
Decision Date2017-10-02
Product CodeEBI
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

Nobilplast Denture Resin is a medical device manufactured by Cmp Industries, LLC. It received FDA 510(k) clearance on 2017-10-02 under approval number K170375. The device is classified under product code EBI. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Nobilplast Denture Resin?

Nobilplast Denture Resin is a medical device that received FDA 510(k) clearance on 2017-10-02. It is manufactured by Cmp Industries, LLC. The 510(k) number is K170375.

When was Nobilplast Denture Resin approved by the FDA?

Nobilplast Denture Resin received FDA 510(k) clearance on 2017-10-02, under approval number K170375.

What company makes Nobilplast Denture Resin?

Nobilplast Denture Resin is manufactured by Cmp Industries, LLC.

What is the FDA product code for Nobilplast Denture Resin?

The FDA product code for Nobilplast Denture Resin is EBI.

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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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