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FDA 510(k)

VERACIA SA

K-Number: K113426 · 2012-02-08

ApplicantShofu Dental Corporation
Decision Date2012-02-08
Product CodeELM
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

VERACIA SA is the device name listed in this FDA 510(k) record. The listed applicant is Shofu Dental Corporation. It received FDA 510(k) clearance on 2012-02-08 under 510(k) number K113426. The device is classified under product code ELM. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VERACIA SA?

VERACIA SA is a medical device that received FDA 510(k) clearance on 2012-02-08. The listed applicant is Shofu Dental Corporation. The 510(k) number is K113426.

When did VERACIA SA receive FDA 510(k) clearance?

VERACIA SA received FDA 510(k) clearance on 2012-02-08, under 510(k) number K113426.

Who is the listed applicant for VERACIA SA?

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

What is the FDA product code for VERACIA SA?

The FDA product code for VERACIA SA is ELM.

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Other records listing Shofu Dental Corporation 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.

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Related Devices (Code: ELM)

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.

K122955DENTAVIT, MONARCH, ACROTONE, SENATOR, DENTORIUMWright Health Group , Ltd.K122925NEW STETIC ARTIFICIAL TEETHNew SteticK122852PHYSIOSTAR NFCCandulor USA, Inc.K121749VERACIAShofu Dental CorporationK120404MERZ DENTAL GMBH ARTEGRAL HD PREFORMED PLASTIC DENTURE TEETHMerz Dental GmbHK120736SR PHONARES IIIvoclar Vivadent, AG

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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