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FDA 510(k)

ULTRACROWN(TM) PD ALLOY POST-SOLDER

K-Number: K913860 · 1991-11-13

ApplicantDentsply Intl.
Decision Date1991-11-13
Product CodeEJS
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

ULTRACROWN(TM) PD ALLOY POST-SOLDER is the device name listed in this FDA 510(k) record. The listed applicant is Dentsply Intl.. It received FDA 510(k) clearance on 1991-11-13 under 510(k) number K913860. 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 ULTRACROWN(TM) PD ALLOY POST-SOLDER?

ULTRACROWN(TM) PD ALLOY POST-SOLDER is a medical device that received FDA 510(k) clearance on 1991-11-13. The listed applicant is Dentsply Intl.. The 510(k) number is K913860.

When did ULTRACROWN(TM) PD ALLOY POST-SOLDER receive FDA 510(k) clearance?

ULTRACROWN(TM) PD ALLOY POST-SOLDER received FDA 510(k) clearance on 1991-11-13, under 510(k) number K913860.

Who is the listed applicant for ULTRACROWN(TM) PD ALLOY POST-SOLDER?

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 ULTRACROWN(TM) PD ALLOY POST-SOLDER?

The FDA product code for ULTRACROWN(TM) PD ALLOY POST-SOLDER is EJS.

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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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