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)

UCLA AND CEMENT-ON ABUTMENTS AND ACCESSORIES

K-Number: K034022 · 2004-01-30

ApplicantDiamodent
Decision Date2004-01-30
Product CodeDZE
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

UCLA AND CEMENT-ON ABUTMENTS AND ACCESSORIES is the device name listed in this FDA 510(k) record. The listed applicant is Diamodent. It received FDA 510(k) clearance on 2004-01-30 under 510(k) number K034022. 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 UCLA AND CEMENT-ON ABUTMENTS AND ACCESSORIES?

UCLA AND CEMENT-ON ABUTMENTS AND ACCESSORIES is a medical device that received FDA 510(k) clearance on 2004-01-30. The listed applicant is Diamodent. The 510(k) number is K034022.

When did UCLA AND CEMENT-ON ABUTMENTS AND ACCESSORIES receive FDA 510(k) clearance?

UCLA AND CEMENT-ON ABUTMENTS AND ACCESSORIES received FDA 510(k) clearance on 2004-01-30, under 510(k) number K034022.

Who is the listed applicant for UCLA AND CEMENT-ON ABUTMENTS AND ACCESSORIES?

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

What is the FDA product code for UCLA AND CEMENT-ON ABUTMENTS AND ACCESSORIES?

The FDA product code for UCLA AND CEMENT-ON ABUTMENTS AND ACCESSORIES 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 Diamodent 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.

K010619UCLA AND UNIVERSAL ABUTMENTSK993129UCLA/UNIVERSAL ABUTMENT

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.

↑