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FDA 510(k)

STABILIZING RETAINER

K-Number: K843143 · 1984-09-27

ApplicantDental Advancements, Inc.
Decision Date1984-09-27
Product CodeEJF
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

STABILIZING RETAINER is the device name listed in this FDA 510(k) record. The listed applicant is Dental Advancements, Inc.. It received FDA 510(k) clearance on 1984-09-27 under 510(k) number K843143. 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 STABILIZING RETAINER?

STABILIZING RETAINER is a medical device that received FDA 510(k) clearance on 1984-09-27. The listed applicant is Dental Advancements, Inc.. The 510(k) number is K843143.

When did STABILIZING RETAINER receive FDA 510(k) clearance?

STABILIZING RETAINER received FDA 510(k) clearance on 1984-09-27, under 510(k) number K843143.

Who is the listed applicant for STABILIZING RETAINER?

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

What is the FDA product code for STABILIZING RETAINER?

The FDA product code for STABILIZING RETAINER is EJF.

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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.

K994357BITEM LOCK, MODELS SW006, SW012Thermoelastic Technologies, Inc.K932825MICROARCH GOLD BRACKETGac Intl., Inc.K933501ALASTIKUnitek Corp.K923372MEMORY WIREAlthan, Inc.K933080ORTHOTECH DURA-GOLD BARCKETSOrthotechK935139FASCINATION CERAMIC BRACKETDentauraum, Inc.

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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