BONART ART-L3 LED CURING LIGHT
K-Number: K062289 · 2007-01-03
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Device Summary
Frequently Asked Questions
What is the BONART ART-L3 LED CURING LIGHT?
BONART ART-L3 LED CURING LIGHT is a medical device that received FDA 510(k) clearance on 2007-01-03. The listed applicant is Bonart Co., Ltd.. The 510(k) number is K062289.
When did BONART ART-L3 LED CURING LIGHT receive FDA 510(k) clearance?
BONART ART-L3 LED CURING LIGHT received FDA 510(k) clearance on 2007-01-03, under 510(k) number K062289.
Who is the listed applicant for BONART ART-L3 LED CURING LIGHT?
The FDA 510(k) record lists Bonart Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for BONART ART-L3 LED CURING LIGHT?
The FDA product code for BONART ART-L3 LED CURING LIGHT 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 Bonart Co., Ltd. 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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