UNIOLITE
K-Number: K771889 · 1977-10-20
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Device Summary
Frequently Asked Questions
What is the UNIOLITE?
UNIOLITE is a medical device that received FDA 510(k) clearance on 1977-10-20. The listed applicant is Espe Dental Products. The 510(k) number is K771889.
When did UNIOLITE receive FDA 510(k) clearance?
UNIOLITE received FDA 510(k) clearance on 1977-10-20, under 510(k) number K771889.
Who is the listed applicant for UNIOLITE?
The FDA 510(k) record lists Espe Dental Products as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for UNIOLITE?
The FDA product code for UNIOLITE 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 Products 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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