Etgar Dental Implant System
K-Number: K161743 · 2017-04-14
Device Summary
Frequently Asked Questions
What is the Etgar Dental Implant System?
Etgar Dental Implant System is a medical device that received FDA 510(k) clearance on 2017-04-14. The listed applicant is Etgar Medical Instruments, Ltd.. The 510(k) number is K161743.
When did Etgar Dental Implant System receive FDA 510(k) clearance?
Etgar Dental Implant System received FDA 510(k) clearance on 2017-04-14, under 510(k) number K161743.
Who is the listed applicant for Etgar Dental Implant System?
The FDA 510(k) record lists Etgar Medical Instruments, Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Etgar Dental Implant System?
The FDA product code for Etgar Dental Implant System is DZE.
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.