DEN TEK COMFORT FIT NIGHTGUARD
K-Number: K072147 · 2007-08-30
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Device Summary
Frequently Asked Questions
What is the DEN TEK COMFORT FIT NIGHTGUARD?
DEN TEK COMFORT FIT NIGHTGUARD is a medical device that received FDA 510(k) clearance on 2007-08-30. The listed applicant is Den Tek Oral Care, Inc.. The 510(k) number is K072147.
When did DEN TEK COMFORT FIT NIGHTGUARD receive FDA 510(k) clearance?
DEN TEK COMFORT FIT NIGHTGUARD received FDA 510(k) clearance on 2007-08-30, under 510(k) number K072147.
Who is the listed applicant for DEN TEK COMFORT FIT NIGHTGUARD?
The FDA 510(k) record lists Den Tek Oral Care, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for DEN TEK COMFORT FIT NIGHTGUARD?
The FDA product code for DEN TEK COMFORT FIT NIGHTGUARD is OBR. This falls under the Orthopedic category.
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 Den Tek Oral Care, 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: OBR)
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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