LEONE ORTHODONTIC MINI IMPLANT
K-Number: K071490 · 2008-02-22
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Device Summary
Frequently Asked Questions
What is the LEONE ORTHODONTIC MINI IMPLANT?
LEONE ORTHODONTIC MINI IMPLANT is a medical device that received FDA 510(k) clearance on 2008-02-22. The listed applicant is Leone S.P.A.. The 510(k) number is K071490.
When did LEONE ORTHODONTIC MINI IMPLANT receive FDA 510(k) clearance?
LEONE ORTHODONTIC MINI IMPLANT received FDA 510(k) clearance on 2008-02-22, under 510(k) number K071490.
Who is the listed applicant for LEONE ORTHODONTIC MINI IMPLANT?
The FDA 510(k) record lists Leone S.P.A. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for LEONE ORTHODONTIC MINI IMPLANT?
The FDA product code for LEONE ORTHODONTIC MINI IMPLANT is OAT.
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 Leone S.P.A. 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: OAT)
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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