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FDA 510(k)

PRECISE DENTURE BASE RESIN

K-Number: K952351 · 1995-07-07

ApplicantDentsply Intl.
Decision Date1995-07-07
Product CodeEBI
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

PRECISE DENTURE BASE RESIN is the device name listed in this FDA 510(k) record. The listed applicant is Dentsply Intl.. It received FDA 510(k) clearance on 1995-07-07 under 510(k) number K952351. 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 PRECISE DENTURE BASE RESIN?

PRECISE DENTURE BASE RESIN is a medical device that received FDA 510(k) clearance on 1995-07-07. The listed applicant is Dentsply Intl.. The 510(k) number is K952351.

When did PRECISE DENTURE BASE RESIN receive FDA 510(k) clearance?

PRECISE DENTURE BASE RESIN received FDA 510(k) clearance on 1995-07-07, under 510(k) number K952351.

Who is the listed applicant for PRECISE DENTURE BASE RESIN?

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

What is the FDA product code for PRECISE DENTURE BASE RESIN?

The FDA product code for PRECISE DENTURE BASE RESIN is EBI.

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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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