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FDA 510(k)

RIVA BOND LC

K-Number: K062064 · 2006-11-09

ApplicantSouthern Dental Industries, Inc.
Decision Date2006-11-09
Product CodeEMA
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

RIVA BOND LC is the device name listed in this FDA 510(k) record. The listed applicant is Southern Dental Industries, Inc.. It received FDA 510(k) clearance on 2006-11-09 under 510(k) number K062064. The device is classified under product code EMA. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RIVA BOND LC?

RIVA BOND LC is a medical device that received FDA 510(k) clearance on 2006-11-09. The listed applicant is Southern Dental Industries, Inc.. The 510(k) number is K062064.

When did RIVA BOND LC receive FDA 510(k) clearance?

RIVA BOND LC received FDA 510(k) clearance on 2006-11-09, under 510(k) number K062064.

Who is the listed applicant for RIVA BOND LC?

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

What is the FDA product code for RIVA BOND LC?

The FDA product code for RIVA BOND LC is EMA.

Other records listing Southern Dental Industries, 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: EMA)

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.

K262983EsTemp ImplantSpident Co., Ltd.K254201Any-CemMediclus Co., Ltd.K261937PacTemp Automix NEThe Belport Company Inc., DBA Gingi-PakK261166DIA-CEMDiaDent Group InternationalK254109G-CEM UNIVERSALGC America, Inc.K253337REGEN Bioactive CementInter-Med, 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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