ELIPAR TRILIGHT
K-Number: K984247 · 1999-02-25
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Device Summary
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.
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.
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