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FDA 510(k)

TOKUYAMA TISSUECARE

K-Number: K081554 · 2009-03-18

ApplicantTokuyama Dental Corporation
Decision Date2009-03-18
Product CodeEBI
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

TOKUYAMA TISSUECARE is the device name listed in this FDA 510(k) record. The listed applicant is Tokuyama Dental Corporation. It received FDA 510(k) clearance on 2009-03-18 under 510(k) number K081554. The device is classified under product code EBI. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TOKUYAMA TISSUECARE?

TOKUYAMA TISSUECARE is a medical device that received FDA 510(k) clearance on 2009-03-18. The listed applicant is Tokuyama Dental Corporation. The 510(k) number is K081554.

When did TOKUYAMA TISSUECARE receive FDA 510(k) clearance?

TOKUYAMA TISSUECARE received FDA 510(k) clearance on 2009-03-18, under 510(k) number K081554.

Who is the listed applicant for TOKUYAMA TISSUECARE?

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

What is the FDA product code for TOKUYAMA TISSUECARE?

The FDA product code for TOKUYAMA TISSUECARE is EBI.

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Other records listing Tokuyama 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.

K203760Tokuyama Universal Bond IIK203598Omnichroma Flow BulkK193537Omnichroma FlowK190940Tokuyama Rebase IIIK180613Estelite Universal FlowK173275OMNICHROMA

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Related Devices (Code: EBI)

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.

K261802Glidewell™ Denture Base ResinPrismatik Dentalcraft, Inc.K261626UltraPrint Flexible Denture UVGuangzhou Heygears IMC., Inc.K262681NanoCeram Resin3BFAB TEKNOLOJI A.S.K262300Denture Base Resin V2Formlabs Ohio, Inc.K261474DENTCA Tru FlexibleDentca, Inc.K260569DB 4000 High Impact Denture BaseCarbon, Inc.

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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