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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 the device name listed in this FDA 510(k) record. The listed applicant is Inter-Med / Vista Dental. It received FDA 510(k) clearance on 2021-08-18 under 510(k) 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. The listed applicant is Inter-Med / Vista Dental. The 510(k) number is K211813.

When did Triton receive FDA 510(k) clearance?

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

Who is the listed applicant for Triton?

The FDA 510(k) record lists Inter-Med / Vista Dental as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Triton?

The FDA product code for Triton is KJJ.

Related Devices (Code: KJJ)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K250279RC-SwiftPrepBelport Company, Inc., Gingi-PakK241354Sealer SolventInter-Med, Inc.K201785EPIEN Dental CleanserEpien Medical, Inc.K193357V-MixInter-Med/Vista Dental ProductsK193409Vista Rinse, Vista Rinse PlusInter-Med/Vista Dental ProductsK200330RC-Prime Root Canal Preparation CreamPac-Dent, Inc.

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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