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FDA 510(k)

DENTAURUM METAL BRACKETS

K-Number: K935122 · 1994-01-31

Decision Date1994-01-31
Product CodeEJF
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

DENTAURUM METAL BRACKETS is the device name listed in this FDA 510(k) record. The listed applicant is Dentauraum, Inc.. It received FDA 510(k) clearance on 1994-01-31 under 510(k) number K935122. The device is classified under product code EJF. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DENTAURUM METAL BRACKETS?

DENTAURUM METAL BRACKETS is a medical device that received FDA 510(k) clearance on 1994-01-31. The listed applicant is Dentauraum, Inc.. The 510(k) number is K935122.

When did DENTAURUM METAL BRACKETS receive FDA 510(k) clearance?

DENTAURUM METAL BRACKETS received FDA 510(k) clearance on 1994-01-31, under 510(k) number K935122.

Who is the listed applicant for DENTAURUM METAL BRACKETS?

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

What is the FDA product code for DENTAURUM METAL BRACKETS?

The FDA product code for DENTAURUM METAL BRACKETS is EJF.

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 Dentauraum, 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 24 devices →

Related Devices (Code: EJF)

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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