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FDA 510(k)

DEGUBOND LITE

K-Number: K912493 · 1991-08-20

ApplicantDegussa AG
Decision Date1991-08-20
Product CodeEJS
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

DEGUBOND LITE is the device name listed in this FDA 510(k) record. The listed applicant is Degussa AG. It received FDA 510(k) clearance on 1991-08-20 under 510(k) number K912493. 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 DEGUBOND LITE?

DEGUBOND LITE is a medical device that received FDA 510(k) clearance on 1991-08-20. The listed applicant is Degussa AG. The 510(k) number is K912493.

When did DEGUBOND LITE receive FDA 510(k) clearance?

DEGUBOND LITE received FDA 510(k) clearance on 1991-08-20, under 510(k) number K912493.

Who is the listed applicant for DEGUBOND LITE?

The FDA 510(k) record lists Degussa AG as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DEGUBOND LITE?

The FDA product code for DEGUBOND LITE is EJS.

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Other records listing Degussa AG 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.

K953344DEGUBOND ULTRAK931808DUCERAGOLD, DUCERATINK926347DUCERANIUM UK922790DEGUCAST 40K921772BIOLORK921479DUCERATIN/DUCERAM LFC DENTAL PORCELAIN

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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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