Symetri Clear
K-Number: K172845 · 2018-01-31
ApplicantOrmco Corporation
Decision Date2018-01-31
Product CodeNJM
Advisory CommitteeDE
DecisionSubstantially Equivalent
Device Summary
Symetri Clear is a medical device manufactured by Ormco Corporation. It received FDA 510(k) clearance on 2018-01-31 under approval number K172845. The device is classified under product code NJM. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Symetri Clear?
Symetri Clear is a medical device that received FDA 510(k) clearance on 2018-01-31. It is manufactured by Ormco Corporation. The 510(k) number is K172845.
When was Symetri Clear approved by the FDA?
Symetri Clear received FDA 510(k) clearance on 2018-01-31, under approval number K172845.
What company makes Symetri Clear?
Symetri Clear is manufactured by Ormco Corporation.
What is the FDA product code for Symetri Clear?
The FDA product code for Symetri Clear is NJM.
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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.