DENTRIa series
K-Number: K160140 · 2016-09-30
ApplicantHdx Will Corp.
Decision Date2016-09-30
Product CodeOAS
Advisory CommitteeRA
DecisionSubstantially Equivalent
Device Summary
DENTRIa series is a medical device manufactured by Hdx Will Corp.. It received FDA 510(k) clearance on 2016-09-30 under approval number K160140. The device is classified under product code OAS. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the DENTRIa series?
DENTRIa series is a medical device that received FDA 510(k) clearance on 2016-09-30. It is manufactured by Hdx Will Corp.. The 510(k) number is K160140.
When was DENTRIa series approved by the FDA?
DENTRIa series received FDA 510(k) clearance on 2016-09-30, under approval number K160140.
What company makes DENTRIa series?
DENTRIa series is manufactured by Hdx Will Corp..
What is the FDA product code for DENTRIa series?
The FDA product code for DENTRIa series is OAS.
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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.