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)

ELIPAR TRILIGHT

K-Number: K984247 · 1999-02-25

Decision Date1999-02-25
Product CodeEBZ
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

ELIPAR TRILIGHT is the device name listed in this FDA 510(k) record. The listed applicant is Espe Dental AG. It received FDA 510(k) clearance on 1999-02-25 under 510(k) number K984247. The device is classified under product code EBZ. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ELIPAR TRILIGHT?

ELIPAR TRILIGHT is a medical device that received FDA 510(k) clearance on 1999-02-25. The listed applicant is Espe Dental AG. The 510(k) number is K984247.

When did ELIPAR TRILIGHT receive FDA 510(k) clearance?

ELIPAR TRILIGHT received FDA 510(k) clearance on 1999-02-25, under 510(k) number K984247.

Who is the listed applicant for ELIPAR TRILIGHT?

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

What is the FDA product code for ELIPAR TRILIGHT?

The FDA product code for ELIPAR TRILIGHT is EBZ.

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.

Other records listing Espe Dental 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.

View all 29 devices →

Related Devices (Code: EBZ)

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.

↑