J2A SLA Dental Implant System
K-Number: K161923 · 2017-11-09
Device Summary
Frequently Asked Questions
What is the J2A SLA Dental Implant System?
J2A SLA Dental Implant System is a medical device that received FDA 510(k) clearance on 2017-11-09. The listed applicant is Kj Meditech Co., Ltd.. The 510(k) number is K161923.
When did J2A SLA Dental Implant System receive FDA 510(k) clearance?
J2A SLA Dental Implant System received FDA 510(k) clearance on 2017-11-09, under 510(k) number K161923.
Who is the listed applicant for J2A SLA Dental Implant System?
The FDA 510(k) record lists Kj Meditech Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for J2A SLA Dental Implant System?
The FDA product code for J2A SLA Dental Implant System is DZE.
Related Clinical Trials
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.
Other records listing Kj Meditech Co., Ltd. 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: 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.