TRI-matrix® X-Force Implants
K-Number: K242661 · 2025-01-08
ApplicantTri Dental Implants Int. AG
Decision Date2025-01-08
Product CodeDZE
Advisory CommitteeDE
DecisionSubstantially Equivalent
Device Summary
TRI-matrix® X-Force Implants is a medical device manufactured by Tri Dental Implants Int. AG. It received FDA 510(k) clearance on 2025-01-08 under approval number K242661. 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 TRI-matrix® X-Force Implants?
TRI-matrix® X-Force Implants is a medical device that received FDA 510(k) clearance on 2025-01-08. It is manufactured by Tri Dental Implants Int. AG. The 510(k) number is K242661.
When was TRI-matrix® X-Force Implants approved by the FDA?
TRI-matrix® X-Force Implants received FDA 510(k) clearance on 2025-01-08, under approval number K242661.
What company makes TRI-matrix® X-Force Implants?
TRI-matrix® X-Force Implants is manufactured by Tri Dental Implants Int. AG.
What is the FDA product code for TRI-matrix® X-Force Implants?
The FDA product code for TRI-matrix® X-Force Implants is DZE.
Related Clinical Trials
Other Devices by Tri Dental Implants Int. AG
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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.