VERINOR ALLOY
K-Number: K864306 · 1986-11-26
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Device Summary
Frequently Asked Questions
What is the VERINOR ALLOY?
VERINOR ALLOY is a medical device that received FDA 510(k) clearance on 1986-11-26. The listed applicant is Degussa Dental, Inc.. The 510(k) number is K864306.
When did VERINOR ALLOY receive FDA 510(k) clearance?
VERINOR ALLOY received FDA 510(k) clearance on 1986-11-26, under 510(k) number K864306.
Who is the listed applicant for VERINOR ALLOY?
The FDA 510(k) record lists Degussa Dental, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for VERINOR ALLOY?
The FDA product code for VERINOR ALLOY is EJT.
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 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: EJT)
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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