CONICAL CONNECTION IMPLANTS
K-Number: K112162 · 2012-08-08
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Device Summary
Frequently Asked Questions
What is the CONICAL CONNECTION IMPLANTS?
CONICAL CONNECTION IMPLANTS is a medical device that received FDA 510(k) clearance on 2012-08-08. The listed applicant is Mis Implants Technologies , Ltd.. The 510(k) number is K112162.
When did CONICAL CONNECTION IMPLANTS receive FDA 510(k) clearance?
CONICAL CONNECTION IMPLANTS received FDA 510(k) clearance on 2012-08-08, under 510(k) number K112162.
Who is the listed applicant for CONICAL CONNECTION IMPLANTS?
The FDA 510(k) record lists Mis Implants Technologies , Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CONICAL CONNECTION IMPLANTS?
The FDA product code for CONICAL CONNECTION 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 Mis Implants Technologies , Ltd. 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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