OSTEOMED ORTHODONTIC ANCHOR PLATING SYSTEM
K-Number: K051798 · 2006-04-07
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Device Summary
Frequently Asked Questions
What is the OSTEOMED ORTHODONTIC ANCHOR PLATING SYSTEM?
OSTEOMED ORTHODONTIC ANCHOR PLATING SYSTEM is a medical device that received FDA 510(k) clearance on 2006-04-07. The listed applicant is Osteomed LP. The 510(k) number is K051798.
When did OSTEOMED ORTHODONTIC ANCHOR PLATING SYSTEM receive FDA 510(k) clearance?
OSTEOMED ORTHODONTIC ANCHOR PLATING SYSTEM received FDA 510(k) clearance on 2006-04-07, under 510(k) number K051798.
Who is the listed applicant for OSTEOMED ORTHODONTIC ANCHOR PLATING SYSTEM?
The FDA 510(k) record lists Osteomed LP as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for OSTEOMED ORTHODONTIC ANCHOR PLATING SYSTEM?
The FDA product code for OSTEOMED ORTHODONTIC ANCHOR PLATING SYSTEM is DZE.
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 Osteomed LP 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: DZE)
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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