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FDA 510(k)

TI-CORE NEW & IMPROVED

K-Number: K922252 · 1994-01-26

ApplicantEssential Dental Systems, Inc.
Decision Date1994-01-26
Product CodeEBF
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

TI-CORE NEW & IMPROVED is the device name listed in this FDA 510(k) record. The listed applicant is Essential Dental Systems, Inc.. It received FDA 510(k) clearance on 1994-01-26 under 510(k) number K922252. The device is classified under product code EBF. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TI-CORE NEW & IMPROVED?

TI-CORE NEW & IMPROVED is a medical device that received FDA 510(k) clearance on 1994-01-26. The listed applicant is Essential Dental Systems, Inc.. The 510(k) number is K922252.

When did TI-CORE NEW & IMPROVED receive FDA 510(k) clearance?

TI-CORE NEW & IMPROVED received FDA 510(k) clearance on 1994-01-26, under 510(k) number K922252.

Who is the listed applicant for TI-CORE NEW & IMPROVED?

The FDA 510(k) record lists Essential Dental Systems, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TI-CORE NEW & IMPROVED?

The FDA product code for TI-CORE NEW & IMPROVED is EBF.

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Other records listing Essential Dental Systems, Inc. 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.

K223340EDS Calculus Softener TURBO CRK152691EDS Universal CementK111541ENDO-EXPRESS (R) HANDPIECEK101504TI-CORE FLOWK072555EDTA PLUSK070401ENDO-CHX

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Related Devices (Code: EBF)

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.

K262982Core·it DualSpident Co., Ltd.K262202Cerasmart ForteGC America, Inc.K261695Flowable Restorative Material (KP-Flow LF, KP-Flow MF, KP-Flow HF)Guilin Kevin Peter Technology Co., Ltd.K261485Tetric plus Fill;Tetric plus FlowIvoclar Vivadent, Inc.K262228Transcend Bulk Fill Flowable CompositeUltradent Products, Inc.K261246SRGC-06GC America, 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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