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FDA 510(k)

ORTHODONTIC CERAMIC BRACKETS

K-Number: K123094 · 2012-12-13

ApplicantTomy, Inc.
Decision Date2012-12-13
Product CodeNJM
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

ORTHODONTIC CERAMIC BRACKETS is the device name listed in this FDA 510(k) record. The listed applicant is Tomy, Inc.. It received FDA 510(k) clearance on 2012-12-13 under 510(k) number K123094. The device is classified under product code NJM. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ORTHODONTIC CERAMIC BRACKETS?

ORTHODONTIC CERAMIC BRACKETS is a medical device that received FDA 510(k) clearance on 2012-12-13. The listed applicant is Tomy, Inc.. The 510(k) number is K123094.

When did ORTHODONTIC CERAMIC BRACKETS receive FDA 510(k) clearance?

ORTHODONTIC CERAMIC BRACKETS received FDA 510(k) clearance on 2012-12-13, under 510(k) number K123094.

Who is the listed applicant for ORTHODONTIC CERAMIC BRACKETS?

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

What is the FDA product code for ORTHODONTIC CERAMIC BRACKETS?

The FDA product code for ORTHODONTIC CERAMIC BRACKETS is NJM.

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 Tomy, 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: NJM)

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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