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FDA 510(k)

CENTRIX'S ENCORE NATURAL COMPOSITE RESIN CORE PAST

K-Number: K932829 · 1994-01-28

ApplicantAlpha-Dent
Decision Date1994-01-28
Product CodeEBF
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

CENTRIX'S ENCORE NATURAL COMPOSITE RESIN CORE PAST is the device name listed in this FDA 510(k) record. The listed applicant is Alpha-Dent. It received FDA 510(k) clearance on 1994-01-28 under 510(k) number K932829. 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 CENTRIX'S ENCORE NATURAL COMPOSITE RESIN CORE PAST?

CENTRIX'S ENCORE NATURAL COMPOSITE RESIN CORE PAST is a medical device that received FDA 510(k) clearance on 1994-01-28. The listed applicant is Alpha-Dent. The 510(k) number is K932829.

When did CENTRIX'S ENCORE NATURAL COMPOSITE RESIN CORE PAST receive FDA 510(k) clearance?

CENTRIX'S ENCORE NATURAL COMPOSITE RESIN CORE PAST received FDA 510(k) clearance on 1994-01-28, under 510(k) number K932829.

Who is the listed applicant for CENTRIX'S ENCORE NATURAL COMPOSITE RESIN CORE PAST?

The FDA 510(k) record lists Alpha-Dent as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CENTRIX'S ENCORE NATURAL COMPOSITE RESIN CORE PAST?

The FDA product code for CENTRIX'S ENCORE NATURAL COMPOSITE RESIN CORE PAST is EBF.

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 Alpha-Dent 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.

K932828CENTRIX'S ENCORE SOLO LIGHT ACTIVATED RESIN COREK932826CENTRIX'S ENCORE COMPOSITE RESIN CORE PASTE W\FLUOK932827ALPHA-DENT CORE BUILDUP PASTEK904813VISIBLE LIGHT CURE COMPOSITE DENTAL RESTOR. MAT.K904812COMPOSITE RESTORATIVE MATERIAL/RADIOPAQUE

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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