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FDA 510(k)

WIROBOND C

K-Number: K032136 · 2003-09-04

ApplicantBego U.S.A.
Decision Date2003-09-04
Product CodeEJH
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

WIROBOND C is the device name listed in this FDA 510(k) record. The listed applicant is Bego U.S.A.. It received FDA 510(k) clearance on 2003-09-04 under 510(k) number K032136. The device is classified under product code EJH. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the WIROBOND C?

WIROBOND C is a medical device that received FDA 510(k) clearance on 2003-09-04. The listed applicant is Bego U.S.A.. The 510(k) number is K032136.

When did WIROBOND C receive FDA 510(k) clearance?

WIROBOND C received FDA 510(k) clearance on 2003-09-04, under 510(k) number K032136.

Who is the listed applicant for WIROBOND C?

The FDA 510(k) record lists Bego U.S.A. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for WIROBOND C?

The FDA product code for WIROBOND C is EJH.

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Other records listing Bego U.S.A. 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.

K033279GOLD DENTAL CASTING ALLOYSK983080AUROLLOYD KFK983082BEGOCER GK983078BEGOPALK983077BIO PONTOSTARK983079PLATINLLOYD 100

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Related Devices (Code: EJH)

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.

K123929BEGOPAL+Bego Bremer Goldschlaegerei Wilh. Herbst GmbH & COK040180CONTINUM VAalba Dent, Inc.K040179CONTINUMAalba Dent, Inc.K033356VERASOFT ESAalba Dent, Inc.K033045DREAM BOND, DREAMCAST CHROME, DREAMCAST V, DREAM FLEXICAST, DREAM LITHECASTAmerican Green Dent. Mfg, Inc.K031627NANO-TICROWNNano-Write Corp.

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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