MIS CONNECT Conical Connection System
K-Number: K193078 · 2020-03-25
ApplicantDentsply Sirona
Decision Date2020-03-25
Product CodeNHA
Advisory CommitteeDE
DecisionSubstantially Equivalent
Device Summary
MIS CONNECT Conical Connection System is a medical device manufactured by Dentsply Sirona. It received FDA 510(k) clearance on 2020-03-25 under approval number K193078. The device is classified under product code NHA. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the MIS CONNECT Conical Connection System?
MIS CONNECT Conical Connection System is a medical device that received FDA 510(k) clearance on 2020-03-25. It is manufactured by Dentsply Sirona. The 510(k) number is K193078.
When was MIS CONNECT Conical Connection System approved by the FDA?
MIS CONNECT Conical Connection System received FDA 510(k) clearance on 2020-03-25, under approval number K193078.
What company makes MIS CONNECT Conical Connection System?
MIS CONNECT Conical Connection System is manufactured by Dentsply Sirona.
What is the FDA product code for MIS CONNECT Conical Connection System?
The FDA product code for MIS CONNECT Conical Connection System is NHA.
Related Clinical Trials
NCT07137455
EDEN Intracardiac Electrogram Recording and Classifying System
ENROLLING_BY_INVITATION
NCT05883202
Effect of the Abutment-Prosthesis Connection on Marginal Bone Loss and Gingival Sealing Around Dental Implants
SUSPENDED
NCT07572318
Pilot Study on the Feasibility of High-energy Collimation With Optimized Geometry on a VERITON™ CZT Camera
NOT_YET_RECRUITING
NCT07568366
AI in Endoscopic Transsphenoidal Surgery
NOT_YET_RECRUITING
NCT07019662
Comparing a Suture-based System for the Removal of Arterial and Veinous ECMO Cannulas to the Standard Approach
RECRUITING
NCT05994209
Testing the Feasibility and Acceptability of Social Media and Digital Therapeutics to Decrease Vaping Behaviors
RECRUITING
Other Devices by Dentsply Sirona
Related Devices (Code: NHA)
K161713Dentium CAD/CAM AbutmentsDentium Co., Ltd.
K160798IPS e.max® Press Abutment Solutions for Viteo Base TiIvoclar Vivadent, AG
K162004PREMIUM Implant Systems SHELTA Implant SystemsSweden & Martina S.P.A.
K153015Transfer & Angled AbutmentOsstem Implant Co., Ltd.
K161435Temporary Snap AbutmentNobel Biocare AB
K160786RODO Abutment SystemRodo Medical, Inc.
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.