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FDA 510(k)

ASCENT DENTAL CLEANSER

K-Number: K070070 · 2007-05-25

Decision Date2007-05-25
Product CodeLBH
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

ASCENT DENTAL CLEANSER is the device name listed in this FDA 510(k) record. The listed applicant is CAO Group, Inc.. It received FDA 510(k) clearance on 2007-05-25 under 510(k) number K070070. The device is classified under product code LBH. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ASCENT DENTAL CLEANSER?

ASCENT DENTAL CLEANSER is a medical device that received FDA 510(k) clearance on 2007-05-25. The listed applicant is CAO Group, Inc.. The 510(k) number is K070070.

When did ASCENT DENTAL CLEANSER receive FDA 510(k) clearance?

ASCENT DENTAL CLEANSER received FDA 510(k) clearance on 2007-05-25, under 510(k) number K070070.

Who is the listed applicant for ASCENT DENTAL CLEANSER?

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

What is the FDA product code for ASCENT DENTAL CLEANSER?

The FDA product code for ASCENT DENTAL CLEANSER is LBH.

Related Clinical Trials

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.

Other records listing CAO Group, 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.

View all 27 devices →

Related Devices (Code: LBH)

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.

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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