saremco print BRIDGETEC
K-Number: K232050 · 2023-11-14
ApplicantSaremco Dental AG
Decision Date2023-11-14
Product CodeEBF
Advisory CommitteeDE
DecisionSubstantially Equivalent
Device Summary
saremco print BRIDGETEC is a medical device manufactured by Saremco Dental AG. It received FDA 510(k) clearance on 2023-11-14 under approval number K232050. The device is classified under product code EBF. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the saremco print BRIDGETEC?
saremco print BRIDGETEC is a medical device that received FDA 510(k) clearance on 2023-11-14. It is manufactured by Saremco Dental AG. The 510(k) number is K232050.
When was saremco print BRIDGETEC approved by the FDA?
saremco print BRIDGETEC received FDA 510(k) clearance on 2023-11-14, under approval number K232050.
What company makes saremco print BRIDGETEC?
saremco print BRIDGETEC is manufactured by Saremco Dental AG.
What is the FDA product code for saremco print BRIDGETEC?
The FDA product code for saremco print BRIDGETEC is EBF.
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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.