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)

BASE, DENTURE, RELINING, REPAIRING, REBASING,RESIN

K-Number: K883799 · 1988-10-20

ApplicantAustenal Dental, Inc.
Decision Date1988-10-20
Product CodeEBI
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

BASE, DENTURE, RELINING, REPAIRING, REBASING,RESIN is the device name listed in this FDA 510(k) record. The listed applicant is Austenal Dental, Inc.. It received FDA 510(k) clearance on 1988-10-20 under 510(k) number K883799. The device is classified under product code EBI. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BASE, DENTURE, RELINING, REPAIRING, REBASING,RESIN?

BASE, DENTURE, RELINING, REPAIRING, REBASING,RESIN is a medical device that received FDA 510(k) clearance on 1988-10-20. The listed applicant is Austenal Dental, Inc.. The 510(k) number is K883799.

When did BASE, DENTURE, RELINING, REPAIRING, REBASING,RESIN receive FDA 510(k) clearance?

BASE, DENTURE, RELINING, REPAIRING, REBASING,RESIN received FDA 510(k) clearance on 1988-10-20, under 510(k) number K883799.

Who is the listed applicant for BASE, DENTURE, RELINING, REPAIRING, REBASING,RESIN?

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

What is the FDA product code for BASE, DENTURE, RELINING, REPAIRING, REBASING,RESIN?

The FDA product code for BASE, DENTURE, RELINING, REPAIRING, REBASING,RESIN is EBI.

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 Austenal Dental, 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.

K890713OVERDENTURE - STUD ATTACHMENTK880875VITALLIUM EQUIPOISE ALLOYK871849LIGHT CURE DENTURE GLAZEK872746VITALLIUM WIREK863630AUSTENAL ACUPAC 20 DENTURE BASE MATERIALK862557AUSTENAL ACUSOFT SOFT LINER

View all 19 devices →

Related Devices (Code: EBI)

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.

K261802Glidewell™ Denture Base ResinPrismatik Dentalcraft, Inc.K261626UltraPrint Flexible Denture UVGuangzhou Heygears IMC., Inc.K262681NanoCeram Resin3BFAB TEKNOLOJI A.S.K262300Denture Base Resin V2Formlabs Ohio, Inc.K261474DENTCA Tru FlexibleDentca, Inc.K260569DB 4000 High Impact Denture BaseCarbon, 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.

↑