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FDA 510(k)

Apex Locator

K-Number: K231990 · 2024-02-13

ApplicantCefla S.C.
Decision Date2024-02-13
Product CodeLQY
DecisionSubstantially Equivalent

Device Summary

Apex Locator is a medical device manufactured by Cefla S.C.. It received FDA 510(k) clearance on 2024-02-13 under approval number K231990. The device is classified under product code LQY. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Apex Locator?

Apex Locator is a medical device that received FDA 510(k) clearance on 2024-02-13. It is manufactured by Cefla S.C.. The 510(k) number is K231990.

When was Apex Locator approved by the FDA?

Apex Locator received FDA 510(k) clearance on 2024-02-13, under approval number K231990.

What company makes Apex Locator?

Apex Locator is manufactured by Cefla S.C..

What is the FDA product code for Apex Locator?

The FDA product code for Apex Locator is LQY.

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Related Devices (Code: LQY)

K151274Dr's FinderGood Doctors Co., Ltd. K181087Apex Locator, DPEX IIIGuilin Woodpecker Medical Instrument Co., Ltd. K171867Dr’s Finder NEOGood Doctors Co., Ltd. K191806Propex IQ Apex LocatorDentsply Sirona K210789EQ-PEXMeta Systems Co., Ltd. K203836BOMEDENT Apex locator, WISMY Apex locatorChangzhou Bomedent Medical Technology 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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