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)

VANISH ORTHODONTIC BRACKET

K-Number: K844067 · 1984-11-23

ApplicantA Company, Inc.
Decision Date1984-11-23
Product CodeEJF
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

VANISH ORTHODONTIC BRACKET is the device name listed in this FDA 510(k) record. The listed applicant is A Company, Inc.. It received FDA 510(k) clearance on 1984-11-23 under 510(k) number K844067. 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 VANISH ORTHODONTIC BRACKET?

VANISH ORTHODONTIC BRACKET is a medical device that received FDA 510(k) clearance on 1984-11-23. The listed applicant is A Company, Inc.. The 510(k) number is K844067.

When did VANISH ORTHODONTIC BRACKET receive FDA 510(k) clearance?

VANISH ORTHODONTIC BRACKET received FDA 510(k) clearance on 1984-11-23, under 510(k) number K844067.

Who is the listed applicant for VANISH ORTHODONTIC BRACKET?

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

What is the FDA product code for VANISH ORTHODONTIC BRACKET?

The FDA product code for VANISH ORTHODONTIC BRACKET 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

Other records listing A Company, Inc. 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.

K897195A-COMPANY ELECTROTHERMAL DEBONDING DEVICE (ETD)K852596A-COMPANY ELASTIC LIGATURE RINGSK852598A-COMPANY SEPARATING ELASTICSK852599A-COMPANY ELASTOMERIC TUBINGK852800A-COMPANY SELF-LIGATING APPLIANCEK852600A-COMPANY ELASTOMERIC CHAIN DISPENSER

View all 14 devices →

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.

↑