Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

APEX LOCATOR BINGO-1020

K-Number: K992233 · 1999-11-30

ApplicantDent Corp. Research & Development
Decision Date1999-11-30
Product CodeLQY
DecisionSubstantially Equivalent

Device Summary

APEX LOCATOR BINGO-1020 is the device name listed in this FDA 510(k) record. The listed applicant is Dent Corp. Research & Development. It received FDA 510(k) clearance on 1999-11-30 under 510(k) number K992233. The device is classified under product code LQY. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the APEX LOCATOR BINGO-1020?

APEX LOCATOR BINGO-1020 is a medical device that received FDA 510(k) clearance on 1999-11-30. The listed applicant is Dent Corp. Research & Development. The 510(k) number is K992233.

When did APEX LOCATOR BINGO-1020 receive FDA 510(k) clearance?

APEX LOCATOR BINGO-1020 received FDA 510(k) clearance on 1999-11-30, under 510(k) number K992233.

Who is the listed applicant for APEX LOCATOR BINGO-1020?

The FDA 510(k) record lists Dent Corp. Research & Development as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for APEX LOCATOR BINGO-1020?

The FDA product code for APEX LOCATOR BINGO-1020 is LQY.

Related Clinical Trials

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Dent Corp. Research & Development 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.

K063659EASY CURING PEN-STYLE LED CURING LIGHTK020206INTRAORAL CAMERA ME-15

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.

↑