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FDA 510(k)

PERIOSRP TOOTH ROOT CONDITIONER WITH NOVAMIN

K-Number: K071267 · 2007-05-18

Decision Date2007-05-18
Product CodeLBH
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

PERIOSRP TOOTH ROOT CONDITIONER WITH NOVAMIN is the device name listed in this FDA 510(k) record. The listed applicant is Novamin Technology, Inc.. It received FDA 510(k) clearance on 2007-05-18 under 510(k) number K071267. 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 PERIOSRP TOOTH ROOT CONDITIONER WITH NOVAMIN?

PERIOSRP TOOTH ROOT CONDITIONER WITH NOVAMIN is a medical device that received FDA 510(k) clearance on 2007-05-18. The listed applicant is Novamin Technology, Inc.. The 510(k) number is K071267.

When did PERIOSRP TOOTH ROOT CONDITIONER WITH NOVAMIN receive FDA 510(k) clearance?

PERIOSRP TOOTH ROOT CONDITIONER WITH NOVAMIN received FDA 510(k) clearance on 2007-05-18, under 510(k) number K071267.

Who is the listed applicant for PERIOSRP TOOTH ROOT CONDITIONER WITH NOVAMIN?

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

What is the FDA product code for PERIOSRP TOOTH ROOT CONDITIONER WITH NOVAMIN?

The FDA product code for PERIOSRP TOOTH ROOT CONDITIONER WITH NOVAMIN 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 Novamin Technology, 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 7 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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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