Ti Link Abutment
K-Number: K232170 · 2024-01-12
ApplicantIzenimplant Co., Ltd.
Decision Date2024-01-12
Product CodeNHA
Advisory CommitteeDE
DecisionSubstantially Equivalent
Device Summary
Ti Link Abutment is a medical device manufactured by Izenimplant Co., Ltd.. It received FDA 510(k) clearance on 2024-01-12 under approval number K232170. The device is classified under product code NHA. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Ti Link Abutment?
Ti Link Abutment is a medical device that received FDA 510(k) clearance on 2024-01-12. It is manufactured by Izenimplant Co., Ltd.. The 510(k) number is K232170.
When was Ti Link Abutment approved by the FDA?
Ti Link Abutment received FDA 510(k) clearance on 2024-01-12, under approval number K232170.
What company makes Ti Link Abutment?
Ti Link Abutment is manufactured by Izenimplant Co., Ltd..
What is the FDA product code for Ti Link Abutment?
The FDA product code for Ti Link Abutment is NHA.
Other Devices by Izenimplant Co., Ltd.
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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.