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FDA 510(k)

FLEXI-POST

K-Number: K843018 · 1984-09-27

ApplicantEssential Dental Systems, Inc.
Decision Date1984-09-27
Product CodeECR
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

FLEXI-POST is the device name listed in this FDA 510(k) record. The listed applicant is Essential Dental Systems, Inc.. It received FDA 510(k) clearance on 1984-09-27 under 510(k) number K843018. The device is classified under product code ECR. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FLEXI-POST?

FLEXI-POST is a medical device that received FDA 510(k) clearance on 1984-09-27. The listed applicant is Essential Dental Systems, Inc.. The 510(k) number is K843018.

When did FLEXI-POST receive FDA 510(k) clearance?

FLEXI-POST received FDA 510(k) clearance on 1984-09-27, under 510(k) number K843018.

Who is the listed applicant for FLEXI-POST?

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

What is the FDA product code for FLEXI-POST?

The FDA product code for FLEXI-POST is ECR.

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Other records listing Essential Dental Systems, Inc. as applicant

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Related Devices (Code: ECR)

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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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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