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FDA 510(k)

MTA ANGELUS

K-Number: K112046 · 2012-01-06

ApplicantAngelus Industria DE Productos Odontologicos
Decision Date2012-01-06
Product CodeKIF
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

MTA ANGELUS is the device name listed in this FDA 510(k) record. The listed applicant is Angelus Industria DE Productos Odontologicos. It received FDA 510(k) clearance on 2012-01-06 under 510(k) number K112046. 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 ANGELUS?

MTA ANGELUS is a medical device that received FDA 510(k) clearance on 2012-01-06. The listed applicant is Angelus Industria DE Productos Odontologicos. The 510(k) number is K112046.

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

MTA ANGELUS received FDA 510(k) clearance on 2012-01-06, under 510(k) number K112046.

Who is the listed applicant for MTA ANGELUS?

The FDA 510(k) record lists Angelus Industria DE Productos Odontologicos as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MTA ANGELUS?

The FDA product code for MTA ANGELUS 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.

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Other records listing Angelus Industria DE Productos Odontologicos 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.

K151047MTA Repair HPK123823INTERLIGK082180PERMA FIBER,MODEL 441; PERMA MESH, MODEL 440

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.

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