FLASH BOND
K-Number: K920781 · 1992-04-21
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Device Summary
Frequently Asked Questions
What is the FLASH BOND?
FLASH BOND is a medical device that received FDA 510(k) clearance on 1992-04-21. The listed applicant is Advanced Orthodontics Systems, Inc.. The 510(k) number is K920781.
When did FLASH BOND receive FDA 510(k) clearance?
FLASH BOND received FDA 510(k) clearance on 1992-04-21, under 510(k) number K920781.
Who is the listed applicant for FLASH BOND?
The FDA 510(k) record lists Advanced Orthodontics Systems, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for FLASH BOND?
The FDA product code for FLASH BOND is DYH.
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 Advanced Orthodontics Systems, Inc. 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: DYH)
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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