s-Clean SQ-SL Implant System Regular
K-Number: K192688 · 2020-02-04
ApplicantDentis Co., Ltd.
Decision Date2020-02-04
Product CodeDZE
Advisory CommitteeDE
DecisionSubstantially Equivalent
Device Summary
s-Clean SQ-SL Implant System Regular is a medical device manufactured by Dentis Co., Ltd.. It received FDA 510(k) clearance on 2020-02-04 under approval number K192688. The device is classified under product code DZE. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the s-Clean SQ-SL Implant System Regular?
s-Clean SQ-SL Implant System Regular is a medical device that received FDA 510(k) clearance on 2020-02-04. It is manufactured by Dentis Co., Ltd.. The 510(k) number is K192688.
When was s-Clean SQ-SL Implant System Regular approved by the FDA?
s-Clean SQ-SL Implant System Regular received FDA 510(k) clearance on 2020-02-04, under approval number K192688.
What company makes s-Clean SQ-SL Implant System Regular?
s-Clean SQ-SL Implant System Regular is manufactured by Dentis Co., Ltd..
What is the FDA product code for s-Clean SQ-SL Implant System Regular?
The FDA product code for s-Clean SQ-SL Implant System Regular is DZE.
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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.