AXENIC DHP DISPOSABLE HIGH-PERFORMANCE HANDPIECE
K-Number: K072754 · 2008-01-25
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Device Summary
Frequently Asked Questions
What is the AXENIC DHP DISPOSABLE HIGH-PERFORMANCE HANDPIECE?
AXENIC DHP DISPOSABLE HIGH-PERFORMANCE HANDPIECE is a medical device that received FDA 510(k) clearance on 2008-01-25. The listed applicant is Axenic Dental, Inc.. The 510(k) number is K072754.
When did AXENIC DHP DISPOSABLE HIGH-PERFORMANCE HANDPIECE receive FDA 510(k) clearance?
AXENIC DHP DISPOSABLE HIGH-PERFORMANCE HANDPIECE received FDA 510(k) clearance on 2008-01-25, under 510(k) number K072754.
Who is the listed applicant for AXENIC DHP DISPOSABLE HIGH-PERFORMANCE HANDPIECE?
The FDA 510(k) record lists Axenic Dental, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for AXENIC DHP DISPOSABLE HIGH-PERFORMANCE HANDPIECE?
The FDA product code for AXENIC DHP DISPOSABLE HIGH-PERFORMANCE HANDPIECE is EFB.
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.
Related Devices (Code: EFB)
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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