Eq-Pex

FDA 510(k) K210789 · Meta Systems Co., Ltd.

Substantially Equivalent

510(k) numberK210789

Submission

Device name
Eq-Pex
Applicant
Meta Systems Co., Ltd.
Seongnam-Si, KR
Received
March 16, 2021
Decision date
October 20, 2021
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
LQY – Locator, Root Apex
Device class
Unclassified

Other 510(k)s with product code LQY

510(k)DeviceApplicantDecision
K252224Apex Locator (FindPex)LQY · Traditional Changzhou Sifary Medical Technology Co., Ltd.04/08/2026SE
K242383Apex LocatorLQY · Traditional Shenzhen Rogin Medical Co., Ltd.03/07/2025SE
K242765Electronic Apex Locator (Alpha Apex I)LQY · Traditional Shenzhen Superline Technology Co., Ltd.01/17/2025SE
K231990Apex LocatorLQY · Traditional Cefla S.C.02/13/2024SE
K232717Apex Locator (AL-Pex), Apex Locator (AL-Pex+)LQY · Traditional Changzhou Haili Medical Co., Ltd.12/22/2023SE
K212178Root Apex LocatorLQY · Traditional Foshan Coxo Medical Instrument Co., Ltd.07/20/2022SE
K203836BOMEDENT Apex locator, WISMY Apex locatorLQY · Traditional Changzhou Bomedent Medical Technology Co.,Ltd03/30/2021SE
K191806Propex IQ Apex LocatorLQY · Traditional Dentsply Sirona10/03/2019SE
K181087Apex Locator, DPEX IIILQY · Traditional Guilin Woodpecker Medical Instrument Co., Ltd.12/18/2018SE
K171867Dr’s Finder NEOLQY · Traditional Good Doctors Co., Ltd.03/30/2018SE

More from Good Doctors Co., Ltd.

510(k)DeviceDecision
K253461Demi ProEBZ · Traditional 10/14/2025SE
K210475Eq-MEKX · Traditional 09/21/2022SE
K153285EMS-200EKX · Traditional 08/12/2016SE

Questions and answers

When was Eq-Pex cleared by the FDA?

Eq-Pex (K210789) received a 510(k) decision of Substantially Equivalent on October 20, 2021, 218 days after the submission was received.

What is the product code of K210789?

The FDA product code is LQY – Locator, Root Apex, a Unclassified device.