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FDA 510(k)

BERNHARD-FORSTER GMBH ORTHODONTIC CERAMIC BRACKETS

K-Number: K090933 · 2009-06-05

ApplicantForestadent Bernhard Forster GmbH
Decision Date2009-06-05
Product CodeNJM
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

BERNHARD-FORSTER GMBH ORTHODONTIC CERAMIC BRACKETS is the device name listed in this FDA 510(k) record. The listed applicant is Forestadent Bernhard Forster GmbH. It received FDA 510(k) clearance on 2009-06-05 under 510(k) number K090933. 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 BERNHARD-FORSTER GMBH ORTHODONTIC CERAMIC BRACKETS?

BERNHARD-FORSTER GMBH ORTHODONTIC CERAMIC BRACKETS is a medical device that received FDA 510(k) clearance on 2009-06-05. The listed applicant is Forestadent Bernhard Forster GmbH. The 510(k) number is K090933.

When did BERNHARD-FORSTER GMBH ORTHODONTIC CERAMIC BRACKETS receive FDA 510(k) clearance?

BERNHARD-FORSTER GMBH ORTHODONTIC CERAMIC BRACKETS received FDA 510(k) clearance on 2009-06-05, under 510(k) number K090933.

Who is the listed applicant for BERNHARD-FORSTER GMBH ORTHODONTIC CERAMIC BRACKETS?

The FDA 510(k) record lists Forestadent Bernhard Forster GmbH as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BERNHARD-FORSTER GMBH ORTHODONTIC CERAMIC BRACKETS?

The FDA product code for BERNHARD-FORSTER GMBH ORTHODONTIC CERAMIC BRACKETS is NJM.

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Other records listing Forestadent Bernhard Forster GmbH 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.

K110275ORTHO EASY PINK925240FACEBOWK924971FORESTADENT BRACKETS

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

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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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