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FDA 510(k)

PITT-EASY DENTAL IMPLANT SYSTEM

K-Number: K053242 · 2006-01-06

Decision Date2006-01-06
Product CodeDZE
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

PITT-EASY DENTAL IMPLANT SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Innova Life Sciences Corp.. It received FDA 510(k) clearance on 2006-01-06 under 510(k) number K053242. 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 PITT-EASY DENTAL IMPLANT SYSTEM?

PITT-EASY DENTAL IMPLANT SYSTEM is a medical device that received FDA 510(k) clearance on 2006-01-06. The listed applicant is Innova Life Sciences Corp.. The 510(k) number is K053242.

When did PITT-EASY DENTAL IMPLANT SYSTEM receive FDA 510(k) clearance?

PITT-EASY DENTAL IMPLANT SYSTEM received FDA 510(k) clearance on 2006-01-06, under 510(k) number K053242.

Who is the listed applicant for PITT-EASY DENTAL IMPLANT SYSTEM?

The FDA 510(k) record lists Innova Life Sciences Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PITT-EASY DENTAL IMPLANT SYSTEM?

The FDA product code for PITT-EASY 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 Life Sciences 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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