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)

LARIAT PALATE EXPANDER

K-Number: K926427 · 1994-01-26

ApplicantEasy Access Orthodontics, Inc.
Decision Date1994-01-26
Product CodeEJF
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

LARIAT PALATE EXPANDER is the device name listed in this FDA 510(k) record. The listed applicant is Easy Access Orthodontics, Inc.. It received FDA 510(k) clearance on 1994-01-26 under 510(k) number K926427. The device is classified under product code EJF. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LARIAT PALATE EXPANDER?

LARIAT PALATE EXPANDER is a medical device that received FDA 510(k) clearance on 1994-01-26. The listed applicant is Easy Access Orthodontics, Inc.. The 510(k) number is K926427.

When did LARIAT PALATE EXPANDER receive FDA 510(k) clearance?

LARIAT PALATE EXPANDER received FDA 510(k) clearance on 1994-01-26, under 510(k) number K926427.

Who is the listed applicant for LARIAT PALATE EXPANDER?

The FDA 510(k) record lists Easy Access Orthodontics, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LARIAT PALATE EXPANDER?

The FDA product code for LARIAT PALATE EXPANDER is EJF.

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

Related Devices (Code: EJF)

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.

K994357BITEM LOCK, MODELS SW006, SW012Thermoelastic Technologies, Inc.K932825MICROARCH GOLD BRACKETGac Intl., Inc.K933501ALASTIKUnitek Corp.K923372MEMORY WIREAlthan, Inc.K933080ORTHOTECH DURA-GOLD BARCKETSOrthotechK935139FASCINATION CERAMIC BRACKETDentauraum, Inc.

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.

↑