BTI INTERNA DENTAL IMPLANT SYSTEM
K-Number: K053355 · 2006-03-14
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Device Summary
Frequently Asked Questions
What is the BTI INTERNA DENTAL IMPLANT SYSTEM?
BTI INTERNA DENTAL IMPLANT SYSTEM is a medical device that received FDA 510(k) clearance on 2006-03-14. The listed applicant is B.T.I. Biotechnology Institute, Sl.. The 510(k) number is K053355.
When did BTI INTERNA DENTAL IMPLANT SYSTEM receive FDA 510(k) clearance?
BTI INTERNA DENTAL IMPLANT SYSTEM received FDA 510(k) clearance on 2006-03-14, under 510(k) number K053355.
Who is the listed applicant for BTI INTERNA DENTAL IMPLANT SYSTEM?
The FDA 510(k) record lists B.T.I. Biotechnology Institute, Sl. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for BTI INTERNA DENTAL IMPLANT SYSTEM?
The FDA product code for BTI INTERNA DENTAL IMPLANT SYSTEM is DZE.
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 B.T.I. Biotechnology Institute, Sl. 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: DZE)
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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