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)

RAVE COMPOSITE BRACKET

K-Number: K052714 · 2005-10-26

ApplicantFDA Agents
Decision Date2005-10-26
Product CodeDYW
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

RAVE COMPOSITE BRACKET is the device name listed in this FDA 510(k) record. The listed applicant is FDA Agents. It received FDA 510(k) clearance on 2005-10-26 under 510(k) number K052714. The device is classified under product code DYW. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RAVE COMPOSITE BRACKET?

RAVE COMPOSITE BRACKET is a medical device that received FDA 510(k) clearance on 2005-10-26. The listed applicant is FDA Agents. The 510(k) number is K052714.

When did RAVE COMPOSITE BRACKET receive FDA 510(k) clearance?

RAVE COMPOSITE BRACKET received FDA 510(k) clearance on 2005-10-26, under 510(k) number K052714.

Who is the listed applicant for RAVE COMPOSITE BRACKET?

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

What is the FDA product code for RAVE COMPOSITE BRACKET?

The FDA product code for RAVE COMPOSITE BRACKET is DYW.

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: DYW)

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.

K252760Carriere® Motion Pro® Clear Bite CorrectorOrtho Organizers, Inc.K251196Composite Orthodontic Brackets and ButtonsEc Certification Service GmbHK201940Braces on Demand BracketBraces on Demand, Inc.K182338Blue Sky Bio Computerized Orthodontic Bracket SystemBlue Sky BioK180718ORTHODONTIC PLASTIC BRACKETS AND ACCESSORIESTomy, Inc.K160720Carriere Motion Clear Class IIOrtho Organizers, 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.

↑