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)

APROXI 1100 AND 4000 SERIES DENTAL INLAYS

K-Number: K073047 · 2008-08-07

ApplicantAproxi Aps
Decision Date2008-08-07
Product CodeEBF
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

APROXI 1100 AND 4000 SERIES DENTAL INLAYS is the device name listed in this FDA 510(k) record. The listed applicant is Aproxi Aps. It received FDA 510(k) clearance on 2008-08-07 under 510(k) number K073047. The device is classified under product code EBF. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the APROXI 1100 AND 4000 SERIES DENTAL INLAYS?

APROXI 1100 AND 4000 SERIES DENTAL INLAYS is a medical device that received FDA 510(k) clearance on 2008-08-07. The listed applicant is Aproxi Aps. The 510(k) number is K073047.

When did APROXI 1100 AND 4000 SERIES DENTAL INLAYS receive FDA 510(k) clearance?

APROXI 1100 AND 4000 SERIES DENTAL INLAYS received FDA 510(k) clearance on 2008-08-07, under 510(k) number K073047.

Who is the listed applicant for APROXI 1100 AND 4000 SERIES DENTAL INLAYS?

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

What is the FDA product code for APROXI 1100 AND 4000 SERIES DENTAL INLAYS?

The FDA product code for APROXI 1100 AND 4000 SERIES DENTAL INLAYS is EBF.

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: EBF)

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.

K262982Core·it DualSpident Co., Ltd.K262202Cerasmart ForteGC America, Inc.K261695Flowable Restorative Material (KP-Flow LF, KP-Flow MF, KP-Flow HF)Guilin Kevin Peter Technology Co., Ltd.K261485Tetric plus Fill;Tetric plus FlowIvoclar Vivadent, Inc.K262228Transcend Bulk Fill Flowable CompositeUltradent Products, Inc.K261246SRGC-06GC America, 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.

↑