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)

BICON TRANSITIONAL IMPLANT (BTI) SYSTEM

K-Number: K023705 · 2003-01-29

ApplicantBicon, Inc.
Decision Date2003-01-29
Product CodeDZE
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

BICON TRANSITIONAL IMPLANT (BTI) SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Bicon, Inc.. It received FDA 510(k) clearance on 2003-01-29 under 510(k) number K023705. The device is classified under product code DZE. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BICON TRANSITIONAL IMPLANT (BTI) SYSTEM?

BICON TRANSITIONAL IMPLANT (BTI) SYSTEM is a medical device that received FDA 510(k) clearance on 2003-01-29. The listed applicant is Bicon, Inc.. The 510(k) number is K023705.

When did BICON TRANSITIONAL IMPLANT (BTI) SYSTEM receive FDA 510(k) clearance?

BICON TRANSITIONAL IMPLANT (BTI) SYSTEM received FDA 510(k) clearance on 2003-01-29, under 510(k) number K023705.

Who is the listed applicant for BICON TRANSITIONAL IMPLANT (BTI) SYSTEM?

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

What is the FDA product code for BICON TRANSITIONAL IMPLANT (BTI) SYSTEM?

The FDA product code for BICON TRANSITIONAL IMPLANT (BTI) SYSTEM is DZE.

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 Bicon, 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.

K062044THE 5.0 X 6.0MM DENTAL IMPLANTK051091SYNTHOGRAFTK0507124.5.* 6.0MM DENTAL IMPLANT AND 6.0*6.0 MM DENTAL IMPLANTK050408BICON ORTHODONTIC IMPLANT SYSTEMK031568BICONITE SURFACE TREATMENTK042637THE 5.0 X 6.0MM DENTAL IMPLANT

View all 13 devices →

Related Devices (Code: DZE)

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.

K261392TriActive Dental Implant SystemParagon Implant Mfg., LLCK260463ZEROS Dental Implant SystemZeros Co., Ltd.K251188UNIQA® Dental Implants SystemUniqa Dental, Ltd.K251232MegaGen Zygoma Dental Implant SystemMegagen Implant Co., Ltd.K250806Dental Implant SystemA.B. Dental Devices , Ltd.K260006INOSS SystemInosys, 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.

↑