CERCON CERAM
K-Number: K011333 · 2001-08-20
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Device Summary
Frequently Asked Questions
What is the CERCON CERAM?
CERCON CERAM is a medical device that received FDA 510(k) clearance on 2001-08-20. The listed applicant is Degussa - Ney Dental, Inc.. The 510(k) number is K011333.
When did CERCON CERAM receive FDA 510(k) clearance?
CERCON CERAM received FDA 510(k) clearance on 2001-08-20, under 510(k) number K011333.
Who is the listed applicant for CERCON CERAM?
The FDA 510(k) record lists Degussa - Ney Dental, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CERCON CERAM?
The FDA product code for CERCON CERAM is EIH.
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 Degussa - Ney Dental, 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: EIH)
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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