DENSHIELD TREATMENT FOR SENSITIVE TEETH
K-Number: K061359 · 2006-10-18
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Device Summary
Frequently Asked Questions
What is the DENSHIELD TREATMENT FOR SENSITIVE TEETH?
DENSHIELD TREATMENT FOR SENSITIVE TEETH is a medical device that received FDA 510(k) clearance on 2006-10-18. The listed applicant is Novamin Technology, Inc.. The 510(k) number is K061359.
When did DENSHIELD TREATMENT FOR SENSITIVE TEETH receive FDA 510(k) clearance?
DENSHIELD TREATMENT FOR SENSITIVE TEETH received FDA 510(k) clearance on 2006-10-18, under 510(k) number K061359.
Who is the listed applicant for DENSHIELD TREATMENT FOR SENSITIVE TEETH?
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 DENSHIELD TREATMENT FOR SENSITIVE TEETH?
The FDA product code for DENSHIELD TREATMENT FOR SENSITIVE TEETH 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.
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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