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FDA 510(k)

GDC 1742 (A CASTING ALLOY FOR DENTAL RESTORATIONS)

K-Number: K860119 · 1986-03-17

ApplicantDeringer-Ney, Inc.
Decision Date1986-03-17
Product CodeEJS
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

GDC 1742 (A CASTING ALLOY FOR DENTAL RESTORATIONS) is the device name listed in this FDA 510(k) record. The listed applicant is Deringer-Ney, Inc.. It received FDA 510(k) clearance on 1986-03-17 under 510(k) number K860119. The device is classified under product code EJS. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GDC 1742 (A CASTING ALLOY FOR DENTAL RESTORATIONS)?

GDC 1742 (A CASTING ALLOY FOR DENTAL RESTORATIONS) is a medical device that received FDA 510(k) clearance on 1986-03-17. The listed applicant is Deringer-Ney, Inc.. The 510(k) number is K860119.

When did GDC 1742 (A CASTING ALLOY FOR DENTAL RESTORATIONS) receive FDA 510(k) clearance?

GDC 1742 (A CASTING ALLOY FOR DENTAL RESTORATIONS) received FDA 510(k) clearance on 1986-03-17, under 510(k) number K860119.

Who is the listed applicant for GDC 1742 (A CASTING ALLOY FOR DENTAL RESTORATIONS)?

The FDA 510(k) record lists Deringer-Ney, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for GDC 1742 (A CASTING ALLOY FOR DENTAL RESTORATIONS)?

The FDA product code for GDC 1742 (A CASTING ALLOY FOR DENTAL RESTORATIONS) is EJS.

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Other records listing Deringer-Ney, 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.

K933178GDC 3509K930481DENTAL CASTING ALLOY MODIFICATION-PF-4K930482DENTAL CASTING ALLOY, MODIFICATION - PF-3K925273GDC 3445K920922GDC 3367K920060DENTAL SOLDER ALLOY

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Related Devices (Code: EJS)

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.

K041433BRIGHT GOLD XHIvoclar Vivadent, Inc.K040436SIMIDUR SUPERIORWieland Dental + Technik GmbH & Co. KGK022252STERNGOLD 1, MODEL 1127781SterngoldK022469ECO E4Wieland Dental + Technik GmbH & Co. KGK021367STERNGOLD 66, MODEL #1180230SterngoldK020195SIMIDUR S1SWieland Dental + Technik GmbH & Co. KG

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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