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FDA 510(k)

EDTA PLUS

K-Number: K072555 · 2007-12-13

Decision Date2007-12-13
Product CodeKJJ
DecisionSubstantially Equivalent

Device Summary

EDTA PLUS 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 2007-12-13 under 510(k) number K072555. The device is classified under product code KJJ. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EDTA PLUS?

EDTA PLUS is a medical device that received FDA 510(k) clearance on 2007-12-13. The listed applicant is Essential Dental Systems, Inc.. The 510(k) number is K072555.

When did EDTA PLUS receive FDA 510(k) clearance?

EDTA PLUS received FDA 510(k) clearance on 2007-12-13, under 510(k) number K072555.

Who is the listed applicant for EDTA PLUS?

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 EDTA PLUS?

The FDA product code for EDTA PLUS is KJJ.

Other records listing Essential Dental Systems, 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 15 devices →

Related Devices (Code: KJJ)

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

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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