Neodent Implant System - Change in the Shelf Life of Neodent Acqua Implants
K-Number: K193592 · 2020-04-28
Device Summary
Frequently Asked Questions
What is the Neodent Implant System - Change in the Shelf Life of Neodent Acqua Implants?
Neodent Implant System - Change in the Shelf Life of Neodent Acqua Implants is a medical device that received FDA 510(k) clearance on 2020-04-28. It is manufactured by Jjgc Industria E Comercio DE Materiais Dentarios S.A.. The 510(k) number is K193592.
When was Neodent Implant System - Change in the Shelf Life of Neodent Acqua Implants approved by the FDA?
Neodent Implant System - Change in the Shelf Life of Neodent Acqua Implants received FDA 510(k) clearance on 2020-04-28, under approval number K193592.
What company makes Neodent Implant System - Change in the Shelf Life of Neodent Acqua Implants?
Neodent Implant System - Change in the Shelf Life of Neodent Acqua Implants is manufactured by Jjgc Industria E Comercio DE Materiais Dentarios S.A..
What is the FDA product code for Neodent Implant System - Change in the Shelf Life of Neodent Acqua Implants?
The FDA product code for Neodent Implant System - Change in the Shelf Life of Neodent Acqua Implants is DZE.
Related Clinical Trials
Related PubMed Literature
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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.