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FDA 510(k)

APX21

K-Number: K073185 · 2008-03-06

ApplicantTechdent Technologies, Ltd.
Decision Date2008-03-06
Product CodeLQY
DecisionSubstantially Equivalent

Device Summary

APX21 is the device name listed in this FDA 510(k) record. The listed applicant is Techdent Technologies, Ltd.. It received FDA 510(k) clearance on 2008-03-06 under 510(k) number K073185. The device is classified under product code LQY. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the APX21?

APX21 is a medical device that received FDA 510(k) clearance on 2008-03-06. The listed applicant is Techdent Technologies, Ltd.. The 510(k) number is K073185.

When did APX21 receive FDA 510(k) clearance?

APX21 received FDA 510(k) clearance on 2008-03-06, under 510(k) number K073185.

Who is the listed applicant for APX21?

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

What is the FDA product code for APX21?

The FDA product code for APX21 is LQY.

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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