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)

MTA CEMENTS

K-Number: K130125 · 2013-07-24

ApplicantS&C Polymer Silicon- Und Composite Spezialitaeten
Decision Date2013-07-24
Product CodeKIF
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

MTA CEMENTS is the device name listed in this FDA 510(k) record. The listed applicant is S&C Polymer Silicon- Und Composite Spezialitaeten. It received FDA 510(k) clearance on 2013-07-24 under 510(k) number K130125. The device is classified under product code KIF. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MTA CEMENTS?

MTA CEMENTS is a medical device that received FDA 510(k) clearance on 2013-07-24. The listed applicant is S&C Polymer Silicon- Und Composite Spezialitaeten. The 510(k) number is K130125.

When did MTA CEMENTS receive FDA 510(k) clearance?

MTA CEMENTS received FDA 510(k) clearance on 2013-07-24, under 510(k) number K130125.

Who is the listed applicant for MTA CEMENTS?

The FDA 510(k) record lists S&C Polymer Silicon- Und Composite Spezialitaeten as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MTA CEMENTS?

The FDA product code for MTA CEMENTS is KIF.

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: KIF)

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.

K262050Vioseal XSpident Co., Ltd.K253909NeoPEX™ Pre-Mixed Obturation PasteNuSmile, Ltd.K261514Calcium Hydroxide Temporary Filling Material (KP-Cal)Guilin Kevin Peter Technology Co., Ltd.K261415Injectable Root Canal Sealer (KP-Root SP)Guilin Kevin Peter Technology Co., Ltd.K253167Any-PasteMediclus Co., Ltd.K252890ZenSeal ProKerr Corporation

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.

↑