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FDA 510(k)

CDB FLIP-SIDE-CLIP BRACKET

K-Number: K091702 · 2009-08-07

ApplicantCdb Corporation
Decision Date2009-08-07
Product CodeNJM
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

CDB FLIP-SIDE-CLIP BRACKET is the device name listed in this FDA 510(k) record. The listed applicant is Cdb Corporation. It received FDA 510(k) clearance on 2009-08-07 under 510(k) number K091702. 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 CDB FLIP-SIDE-CLIP BRACKET?

CDB FLIP-SIDE-CLIP BRACKET is a medical device that received FDA 510(k) clearance on 2009-08-07. The listed applicant is Cdb Corporation. The 510(k) number is K091702.

When did CDB FLIP-SIDE-CLIP BRACKET receive FDA 510(k) clearance?

CDB FLIP-SIDE-CLIP BRACKET received FDA 510(k) clearance on 2009-08-07, under 510(k) number K091702.

Who is the listed applicant for CDB FLIP-SIDE-CLIP BRACKET?

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

What is the FDA product code for CDB FLIP-SIDE-CLIP BRACKET?

The FDA product code for CDB FLIP-SIDE-CLIP BRACKET is NJM.

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Other records listing Cdb Corporation 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.

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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.

K232827LightForce Orthodontic SystemLightforce OrthodonticsK232011CleoAmerican OrthodonticsK231635A-Line AdvancedBiocetec Co., Ltd.K230225DynaFlex Clear Brackets & ButtonsDyna FlexK222847Ceramic Brackets OrthometricOrthometric - Industria E Comercio DE Produtos MedicosK222764LightForce Orthodontic SystemLightforce Orthodontics

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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