Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

INTERFACE BONDING SYSTEM

K-Number: K896769 · 1990-05-15

Decision Date1990-05-15
Product CodeEBF
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

INTERFACE BONDING SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Smile Horizons, Inc.. It received FDA 510(k) clearance on 1990-05-15 under 510(k) number K896769. The device is classified under product code EBF. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INTERFACE BONDING SYSTEM?

INTERFACE BONDING SYSTEM is a medical device that received FDA 510(k) clearance on 1990-05-15. The listed applicant is Smile Horizons, Inc.. The 510(k) number is K896769.

When did INTERFACE BONDING SYSTEM receive FDA 510(k) clearance?

INTERFACE BONDING SYSTEM received FDA 510(k) clearance on 1990-05-15, under 510(k) number K896769.

Who is the listed applicant for INTERFACE BONDING SYSTEM?

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

What is the FDA product code for INTERFACE BONDING SYSTEM?

The FDA product code for INTERFACE BONDING SYSTEM is EBF.

Related Clinical Trials

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.

Related Devices (Code: EBF)

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.

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.

↑