MODIFIED UNI-STICK PLASTIC LIGATURE
K-Number: K902064 · 1990-08-06
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Device Summary
Frequently Asked Questions
What is the MODIFIED UNI-STICK PLASTIC LIGATURE?
MODIFIED UNI-STICK PLASTIC LIGATURE is a medical device that received FDA 510(k) clearance on 1990-08-06. The listed applicant is American Orthodontics. The 510(k) number is K902064.
When did MODIFIED UNI-STICK PLASTIC LIGATURE receive FDA 510(k) clearance?
MODIFIED UNI-STICK PLASTIC LIGATURE received FDA 510(k) clearance on 1990-08-06, under 510(k) number K902064.
Who is the listed applicant for MODIFIED UNI-STICK PLASTIC LIGATURE?
The FDA 510(k) record lists American Orthodontics as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MODIFIED UNI-STICK PLASTIC LIGATURE?
The FDA product code for MODIFIED UNI-STICK PLASTIC LIGATURE is EJF.
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 American Orthodontics 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: EJF)
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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