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)

KAVO EVEREST C-TEMP

K-Number: K063624 · 2007-02-08

ApplicantKavo America
Decision Date2007-02-08
Product CodeEBG
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

KAVO EVEREST C-TEMP is the device name listed in this FDA 510(k) record. The listed applicant is Kavo America. It received FDA 510(k) clearance on 2007-02-08 under 510(k) number K063624. The device is classified under product code EBG. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KAVO EVEREST C-TEMP?

KAVO EVEREST C-TEMP is a medical device that received FDA 510(k) clearance on 2007-02-08. The listed applicant is Kavo America. The 510(k) number is K063624.

When did KAVO EVEREST C-TEMP receive FDA 510(k) clearance?

KAVO EVEREST C-TEMP received FDA 510(k) clearance on 2007-02-08, under 510(k) number K063624.

Who is the listed applicant for KAVO EVEREST C-TEMP?

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

What is the FDA product code for KAVO EVEREST C-TEMP?

The FDA product code for KAVO EVEREST C-TEMP is EBG.

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 Kavo America 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.

K073074KEY LASER III 1243 US WITH DETECTK072262GENTLERAY 980 DIODE LASER SYSTEMK051909DIAGNODENTK030146KAVO KEY LASER 1242 AND KAVO KEY LASER 1243+K050019IN EXAM INTRAORAL DENTAL X-RAY SYSTEMK032081KAVO EVEREST ZS-BLANK MODELS, 42, 20, AND 60

View all 19 devices →

Related Devices (Code: EBG)

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.

K261261Dura-ArchHangzhou SHINING3D Dental Technology Co., Ltd.K253380“FLNT Base” and “FLNT Temp”Liaoning Upcera Co., Ltd.K251271TempFIT Temporary Crown and Bridge ResinRizhao Huge Biomaterials Company, Ltd.K243370DentaTOOTHAsiga Pty, Ltd.K243621Evoblock, PerléonEvoden Indústria Comércio Importação E ExportaçãoK243951TEMP MASTER, PMMA-based dental resinTaiwan Dental Materials Co., Ltd.

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.

↑