OSSEOTITE IOL IMPLANTS AND OSSEOTITE CERTAIN IOL IMPLANTS
K-Number: K031632 · 2003-09-16
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Device Summary
Frequently Asked Questions
What is the OSSEOTITE IOL IMPLANTS AND OSSEOTITE CERTAIN IOL IMPLANTS?
OSSEOTITE IOL IMPLANTS AND OSSEOTITE CERTAIN IOL IMPLANTS is a medical device that received FDA 510(k) clearance on 2003-09-16. The listed applicant is Implant Innovations, Inc.. The 510(k) number is K031632.
When did OSSEOTITE IOL IMPLANTS AND OSSEOTITE CERTAIN IOL IMPLANTS receive FDA 510(k) clearance?
OSSEOTITE IOL IMPLANTS AND OSSEOTITE CERTAIN IOL IMPLANTS received FDA 510(k) clearance on 2003-09-16, under 510(k) number K031632.
Who is the listed applicant for OSSEOTITE IOL IMPLANTS AND OSSEOTITE CERTAIN IOL IMPLANTS?
The FDA 510(k) record lists Implant Innovations, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for OSSEOTITE IOL IMPLANTS AND OSSEOTITE CERTAIN IOL IMPLANTS?
The FDA product code for OSSEOTITE IOL IMPLANTS AND OSSEOTITE CERTAIN IOL IMPLANTS 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 Implant Innovations, 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: 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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