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FDA 510(k)

VERA SOLDER

K-Number: K972533 · 1997-09-05

ApplicantAalba Dent, Inc.
Decision Date1997-09-05
Product CodeEJS
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

VERA SOLDER is the device name listed in this FDA 510(k) record. The listed applicant is Aalba Dent, Inc.. It received FDA 510(k) clearance on 1997-09-05 under 510(k) number K972533. 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 VERA SOLDER?

VERA SOLDER is a medical device that received FDA 510(k) clearance on 1997-09-05. The listed applicant is Aalba Dent, Inc.. The 510(k) number is K972533.

When did VERA SOLDER receive FDA 510(k) clearance?

VERA SOLDER received FDA 510(k) clearance on 1997-09-05, under 510(k) number K972533.

Who is the listed applicant for VERA SOLDER?

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

What is the FDA product code for VERA SOLDER?

The FDA product code for VERA SOLDER is EJS.

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Other records listing Aalba Dent, 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.

K040180CONTINUM VK040179CONTINUMK033356VERASOFT ESK982094VERABOND 2K972971NPG + 2K973265VERABOND 2V

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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 #1180230SterngoldK020194SIMIDUR KF PLUSWieland 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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