BONART ART-L2 LIGHT CURING UNIT
K-Number: K023721 · 2003-01-10
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Device Summary
Frequently Asked Questions
What is the BONART ART-L2 LIGHT CURING UNIT?
BONART ART-L2 LIGHT CURING UNIT is a medical device that received FDA 510(k) clearance on 2003-01-10. The listed applicant is Bonart Co., Ltd.. The 510(k) number is K023721.
When did BONART ART-L2 LIGHT CURING UNIT receive FDA 510(k) clearance?
BONART ART-L2 LIGHT CURING UNIT received FDA 510(k) clearance on 2003-01-10, under 510(k) number K023721.
Who is the listed applicant for BONART ART-L2 LIGHT CURING UNIT?
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-L2 LIGHT CURING UNIT?
The FDA product code for BONART ART-L2 LIGHT CURING UNIT 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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