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)

VINTAGE LD

K-Number: K152392 · 2016-01-08

ApplicantShofu Dental Corporation
Decision Date2016-01-08
Product CodeEIH
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

VINTAGE LD 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 2016-01-08 under 510(k) number K152392. The device is classified under product code EIH. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VINTAGE LD?

VINTAGE LD is a medical device that received FDA 510(k) clearance on 2016-01-08. The listed applicant is Shofu Dental Corporation. The 510(k) number is K152392.

When did VINTAGE LD receive FDA 510(k) clearance?

VINTAGE LD received FDA 510(k) clearance on 2016-01-08, under 510(k) number K152392.

Who is the listed applicant for VINTAGE LD?

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 VINTAGE LD?

The FDA product code for VINTAGE LD is EIH.

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.

K252808GlasIonomer FX-LCK252165ZIRCONOMER PK251470ResiCem EXK251578BEAUTIFIL IIK233161BeautiLink SAK222253GlasIonomer FX ULTRA

View all 23 devices →

Related Devices (Code: EIH)

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.

K262239Obsidian® Press Over ZirconiaPrismatik Dentalcraft, Inc.K261046Dental Zirconia Blank & Coloring LiquidHunan Qinghao Puzhong Technology Co., Ltd.K262195Dandy Ceramic Stain and GlazeZima International Inc., dba DandyK260918Zolid LunarisAmann Girrbach AGK260859Rosetta SM, Rosetta SPHass Corp.K253191DCMhotbond zirconDental Creativ Management GmbH

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.

↑