Neodent Implant System – Custom Abutments
K-Number: K233857 · 2024-05-02
Device Summary
Frequently Asked Questions
What is the Neodent Implant System – Custom Abutments?
Neodent Implant System – Custom Abutments is a medical device that received FDA 510(k) clearance on 2024-05-02. The listed applicant is JJGC Indústria e Comércio de Materiais Dentários S.A.. The 510(k) number is K233857.
When did Neodent Implant System – Custom Abutments receive FDA 510(k) clearance?
Neodent Implant System – Custom Abutments received FDA 510(k) clearance on 2024-05-02, under 510(k) number K233857.
Who is the listed applicant for Neodent Implant System – Custom Abutments?
The FDA 510(k) record lists JJGC Indústria e Comércio de Materiais Dentários S.A. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Neodent Implant System – Custom Abutments?
The FDA product code for Neodent Implant System – Custom Abutments is NHA.
Other records listing JJGC Indústria e Comércio de Materiais Dentários S.A. 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: NHA)
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.