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FDA 510(k)

CUSTOM COMFORT NIGHTGUARD VERSION 2

K-Number: K091660 · 2009-06-12

Decision Date2009-06-12
Product CodeOBR
DecisionSubstantially Equivalent

Device Summary

CUSTOM COMFORT NIGHTGUARD VERSION 2 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 2009-06-12 under 510(k) number K091660. 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 CUSTOM COMFORT NIGHTGUARD VERSION 2?

CUSTOM COMFORT NIGHTGUARD VERSION 2 is a medical device that received FDA 510(k) clearance on 2009-06-12. The listed applicant is Den Tek Oral Care, Inc.. The 510(k) number is K091660.

When did CUSTOM COMFORT NIGHTGUARD VERSION 2 receive FDA 510(k) clearance?

CUSTOM COMFORT NIGHTGUARD VERSION 2 received FDA 510(k) clearance on 2009-06-12, under 510(k) number K091660.

Who is the listed applicant for CUSTOM COMFORT NIGHTGUARD VERSION 2?

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 CUSTOM COMFORT NIGHTGUARD VERSION 2?

The FDA product code for CUSTOM COMFORT NIGHTGUARD VERSION 2 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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