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FDA 510(k)

DENTURE RUBBER BASE MATERIAL

K-Number: K810094 · 1981-02-02

ApplicantBosworth Co.
Decision Date1981-02-02
Product CodeEBI
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

DENTURE RUBBER BASE MATERIAL is the device name listed in this FDA 510(k) record. The listed applicant is Bosworth Co.. It received FDA 510(k) clearance on 1981-02-02 under 510(k) number K810094. 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 DENTURE RUBBER BASE MATERIAL?

DENTURE RUBBER BASE MATERIAL is a medical device that received FDA 510(k) clearance on 1981-02-02. The listed applicant is Bosworth Co.. The 510(k) number is K810094.

When did DENTURE RUBBER BASE MATERIAL receive FDA 510(k) clearance?

DENTURE RUBBER BASE MATERIAL received FDA 510(k) clearance on 1981-02-02, under 510(k) number K810094.

Who is the listed applicant for DENTURE RUBBER BASE MATERIAL?

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

What is the FDA product code for DENTURE RUBBER BASE MATERIAL?

The FDA product code for DENTURE RUBBER BASE MATERIAL is EBI.

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 Bosworth Co. 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.

K991687MODIFICATION TO LINER II: SOFT RELINE LIQUIDK991902LC PIT & FISSURE SEALANTK953119BOSWORTH RESIN II

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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