ENDOPORE DENTAL IMPLANT ABUTMENTS
K-Number: K952434 · 1995-07-19
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Device Summary
Frequently Asked Questions
What is the ENDOPORE DENTAL IMPLANT ABUTMENTS?
ENDOPORE DENTAL IMPLANT ABUTMENTS is a medical device that received FDA 510(k) clearance on 1995-07-19. The listed applicant is Innova Corp.. The 510(k) number is K952434.
When did ENDOPORE DENTAL IMPLANT ABUTMENTS receive FDA 510(k) clearance?
ENDOPORE DENTAL IMPLANT ABUTMENTS received FDA 510(k) clearance on 1995-07-19, under 510(k) number K952434.
Who is the listed applicant for ENDOPORE DENTAL IMPLANT ABUTMENTS?
The FDA 510(k) record lists Innova Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ENDOPORE DENTAL IMPLANT ABUTMENTS?
The FDA product code for ENDOPORE DENTAL IMPLANT ABUTMENTS 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 Innova Corp. 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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