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FDA 510(k)

ENDOPORE ENDOSSEOUS DENTAL IMPLANT SYSTEM

K-Number: K971196 · 1997-05-08

ApplicantInnova Corp.
Decision Date1997-05-08
Product CodeDZE
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

ENDOPORE ENDOSSEOUS DENTAL IMPLANT SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Innova Corp.. It received FDA 510(k) clearance on 1997-05-08 under 510(k) number K971196. The device is classified under product code DZE. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ENDOPORE ENDOSSEOUS DENTAL IMPLANT SYSTEM?

ENDOPORE ENDOSSEOUS DENTAL IMPLANT SYSTEM is a medical device that received FDA 510(k) clearance on 1997-05-08. The listed applicant is Innova Corp.. The 510(k) number is K971196.

When did ENDOPORE ENDOSSEOUS DENTAL IMPLANT SYSTEM receive FDA 510(k) clearance?

ENDOPORE ENDOSSEOUS DENTAL IMPLANT SYSTEM received FDA 510(k) clearance on 1997-05-08, under 510(k) number K971196.

Who is the listed applicant for ENDOPORE ENDOSSEOUS DENTAL IMPLANT SYSTEM?

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 ENDOSSEOUS DENTAL IMPLANT SYSTEM?

The FDA product code for ENDOPORE ENDOSSEOUS DENTAL IMPLANT 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 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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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