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FDA 510(k)

GRADIA GUM

K-Number: K033808 · 2004-02-02

ApplicantGC America, Inc.
Decision Date2004-02-02
Product CodeEBF
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

GRADIA GUM is the device name listed in this FDA 510(k) record. The listed applicant is GC America, Inc.. It received FDA 510(k) clearance on 2004-02-02 under 510(k) number K033808. 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 GRADIA GUM?

GRADIA GUM is a medical device that received FDA 510(k) clearance on 2004-02-02. The listed applicant is GC America, Inc.. The 510(k) number is K033808.

When did GRADIA GUM receive FDA 510(k) clearance?

GRADIA GUM received FDA 510(k) clearance on 2004-02-02, under 510(k) number K033808.

Who is the listed applicant for GRADIA GUM?

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

What is the FDA product code for GRADIA GUM?

The FDA product code for GRADIA GUM is EBF.

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Other records listing GC America, Inc. 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.

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Related Devices (Code: EBF)

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.

K262982Core·it DualSpident Co., Ltd.K262202Cerasmart ForteGC America, Inc.K261695Flowable Restorative Material (KP-Flow LF, KP-Flow MF, KP-Flow HF)Guilin Kevin Peter Technology Co., Ltd.K261485Tetric plus Fill;Tetric plus FlowIvoclar Vivadent, Inc.K262228Transcend Bulk Fill Flowable CompositeUltradent Products, Inc.K261246SRGC-06GC America, 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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