Nuvola
K-Number: K222418 · 2022-10-07
ApplicantGruppo Europeo Ortodonzia Srl
Decision Date2022-10-07
Product CodeNXC
Advisory CommitteeDE
DecisionSubstantially Equivalent
Device Summary
Nuvola is a medical device manufactured by Gruppo Europeo Ortodonzia Srl. It received FDA 510(k) clearance on 2022-10-07 under approval number K222418. The device is classified under product code NXC. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Nuvola?
Nuvola is a medical device that received FDA 510(k) clearance on 2022-10-07. It is manufactured by Gruppo Europeo Ortodonzia Srl. The 510(k) number is K222418.
When was Nuvola approved by the FDA?
Nuvola received FDA 510(k) clearance on 2022-10-07, under approval number K222418.
What company makes Nuvola?
Nuvola is manufactured by Gruppo Europeo Ortodonzia Srl.
What is the FDA product code for Nuvola?
The FDA product code for Nuvola is NXC.
Related Devices (Code: NXC)
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.