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FDA 510(k)

WIRON 99 DENTAL CASTING ALLOY

K-Number: K903538 · 1991-03-15

ApplicantLeach and Dillon Co., Inc.
Decision Date1991-03-15
Product CodeEJH
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

WIRON 99 DENTAL CASTING ALLOY is the device name listed in this FDA 510(k) record. The listed applicant is Leach and Dillon Co., Inc.. It received FDA 510(k) clearance on 1991-03-15 under 510(k) number K903538. 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 WIRON 99 DENTAL CASTING ALLOY?

WIRON 99 DENTAL CASTING ALLOY is a medical device that received FDA 510(k) clearance on 1991-03-15. The listed applicant is Leach and Dillon Co., Inc.. The 510(k) number is K903538.

When did WIRON 99 DENTAL CASTING ALLOY receive FDA 510(k) clearance?

WIRON 99 DENTAL CASTING ALLOY received FDA 510(k) clearance on 1991-03-15, under 510(k) number K903538.

Who is the listed applicant for WIRON 99 DENTAL CASTING ALLOY?

The FDA 510(k) record lists Leach and Dillon Co., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for WIRON 99 DENTAL CASTING ALLOY?

The FDA product code for WIRON 99 DENTAL CASTING ALLOY is EJH.

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Other records listing Leach and Dillon Co., 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.

K903537250 SL DENTAL CASTING ALLOYK895058HIGH FUSING WHITE CERAMIC SOLDERK895059HIGH FUSING YELLOW CERAMIC SOLDERK903484SELECT 20, DENTAL ALLOYK902372SILVER-FREE CERAMIC SOLDER (SFCS)K902373200 SILHOUETTE LINE (SL) CERAMIC SOLDER

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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.K032136WIROBOND CBego U.S.A.

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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