FDA 510(k)

BOND-ON

K-Number: K820955 · 1982-05-05

Decision Date1982-05-05

Product CodeEJS

Advisory CommitteeDE

DecisionSubstantially Equivalent

Device Summary

BOND-ON is the device name listed in this FDA 510(k) record. The listed applicant is J. Aderer, Inc.. It received FDA 510(k) clearance on 1982-05-05 under 510(k) number K820955. 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 BOND-ON?

BOND-ON is a medical device that received FDA 510(k) clearance on 1982-05-05. The listed applicant is J. Aderer, Inc.. The 510(k) number is K820955.

When did BOND-ON receive FDA 510(k) clearance?

BOND-ON received FDA 510(k) clearance on 1982-05-05, under 510(k) number K820955.

Who is the listed applicant for BOND-ON?

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

What is the FDA product code for BOND-ON?

The FDA product code for BOND-ON is EJS.

Other records listing J. Aderer, 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.

K822956G CAST K822957PURCAST K82179882 ALLOY K821832DEGUCAST U K821572DUALLOR 'R'K821590PORS-ON

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Related Devices (Code: EJS)

K041433BRIGHT GOLD XHIvoclar Vivadent, Inc.K040436SIMIDUR SUPERIORWieland Dental + Technik GmbH & Co. KG K022252STERNGOLD 1, MODEL 1127781Sterngold K022469ECO E4Wieland Dental + Technik GmbH & Co. KG K021367STERNGOLD 66, MODEL #1180230Sterngold K020195SIMIDUR S1SWieland Dental + Technik GmbH & Co. KG

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.