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FDA 510(k)

Triton

K-Number: K211813 · 2021-08-18

ApplicantInter-Med / Vista Dental
Decision Date2021-08-18
Product CodeKJJ
DecisionSubstantially Equivalent

Device Summary

Triton is a medical device manufactured by Inter-Med / Vista Dental. It received FDA 510(k) clearance on 2021-08-18 under approval number K211813. The device is classified under product code KJJ. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Triton?

Triton is a medical device that received FDA 510(k) clearance on 2021-08-18. It is manufactured by Inter-Med / Vista Dental. The 510(k) number is K211813.

When was Triton approved by the FDA?

Triton received FDA 510(k) clearance on 2021-08-18, under approval number K211813.

What company makes Triton?

Triton is manufactured by Inter-Med / Vista Dental.

What is the FDA product code for Triton?

The FDA product code for Triton is KJJ.

Related Devices (Code: KJJ)

K160577PacEndo ChlorhexidinePac-Dent International, Inc. K153528PacEndo EDTAPac-Dent International, Inc. K162311Straumann PrefGelInstitut Straumann AG K173163ChlorCid, ChlorCid V, ChlorCid SurfUltradent Products, Inc. K193357V-MixInter-Med/Vista Dental Products K193409Vista Rinse, Vista Rinse PlusInter-Med/Vista Dental Products

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.

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