NOBELCLINICIAN
K-Number: K123976 · 2013-03-26
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Device Summary
Frequently Asked Questions
What is the NOBELCLINICIAN?
NOBELCLINICIAN is a medical device that received FDA 510(k) clearance on 2013-03-26. The listed applicant is Nobel Biocare AB. The 510(k) number is K123976.
When did NOBELCLINICIAN receive FDA 510(k) clearance?
NOBELCLINICIAN received FDA 510(k) clearance on 2013-03-26, under 510(k) number K123976.
Who is the listed applicant for NOBELCLINICIAN?
The FDA 510(k) record lists Nobel Biocare AB as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for NOBELCLINICIAN?
The FDA product code for NOBELCLINICIAN is LLZ.
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 Nobel Biocare AB 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: LLZ)
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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