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FDA 510(k)

Propex IQ Apex Locator

K-Number: K191806 · 2019-10-03

ApplicantDentsply Sirona
Decision Date2019-10-03
Product CodeLQY
DecisionSubstantially Equivalent

Device Summary

Propex IQ Apex Locator is the device name listed in this FDA 510(k) record. The listed applicant is Dentsply Sirona. It received FDA 510(k) clearance on 2019-10-03 under 510(k) number K191806. The device is classified under product code LQY. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Propex IQ Apex Locator?

Propex IQ Apex Locator is a medical device that received FDA 510(k) clearance on 2019-10-03. The listed applicant is Dentsply Sirona. The 510(k) number is K191806.

When did Propex IQ Apex Locator receive FDA 510(k) clearance?

Propex IQ Apex Locator received FDA 510(k) clearance on 2019-10-03, under 510(k) number K191806.

Who is the listed applicant for Propex IQ Apex Locator?

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

What is the FDA product code for Propex IQ Apex Locator?

The FDA product code for Propex IQ Apex Locator is LQY.

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Related Devices (Code: LQY)

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.

K252224Apex Locator (FindPex)Changzhou Sifary Medical Technology Co., Ltd.K242383Apex LocatorShenzhen Rogin Medical Co., Ltd.K242765Electronic Apex Locator (Alpha Apex I)SHENZHEN SUPERLINE TECHNOLOGY CO., LTD.K231990Apex LocatorCefla S.C.K232717Apex Locator (AL-Pex), Apex Locator (AL-Pex+)Changzhou Haili Medical Co., Ltd.K212178Root Apex LocatorFoshan Coxo Medical Instrument Co., Ltd.

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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