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FDA 510(k)

IMPROVED COMFORT-FIT NIGHTGUARD

K-Number: K081669 · 2008-07-10

Decision Date2008-07-10
Product CodeOBR
DecisionSubstantially Equivalent

Device Summary

IMPROVED COMFORT-FIT NIGHTGUARD is the device name listed in this FDA 510(k) record. The listed applicant is Den Tek Oral Care, Inc.. It received FDA 510(k) clearance on 2008-07-10 under 510(k) number K081669. The device is classified under product code OBR. Product code OBR falls under the category of Orthopedic, which includes orthopedic implants, fixation devices, and surgical instruments. Devices in this category are subject to specific FDA regulatory requirements. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the IMPROVED COMFORT-FIT NIGHTGUARD?

IMPROVED COMFORT-FIT NIGHTGUARD is a medical device that received FDA 510(k) clearance on 2008-07-10. The listed applicant is Den Tek Oral Care, Inc.. The 510(k) number is K081669.

When did IMPROVED COMFORT-FIT NIGHTGUARD receive FDA 510(k) clearance?

IMPROVED COMFORT-FIT NIGHTGUARD received FDA 510(k) clearance on 2008-07-10, under 510(k) number K081669.

Who is the listed applicant for IMPROVED 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 IMPROVED COMFORT-FIT NIGHTGUARD?

The FDA product code for IMPROVED 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.

View all 7 devices →

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

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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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