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FDA 510(k)

VeriSplint

K-Number: K190107 · 2019-07-10

ApplicantWhip Mix Corporation
Decision Date2019-07-10
Product CodeMQC
DecisionSubstantially Equivalent

Device Summary

VeriSplint is a medical device manufactured by Whip Mix Corporation. It received FDA 510(k) clearance on 2019-07-10 under approval number K190107. The device is classified under product code MQC. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VeriSplint?

VeriSplint is a medical device that received FDA 510(k) clearance on 2019-07-10. It is manufactured by Whip Mix Corporation. The 510(k) number is K190107.

When was VeriSplint approved by the FDA?

VeriSplint received FDA 510(k) clearance on 2019-07-10, under approval number K190107.

What company makes VeriSplint?

VeriSplint is manufactured by Whip Mix Corporation.

What is the FDA product code for VeriSplint?

The FDA product code for VeriSplint is MQC.

Other Devices by Whip Mix Corporation

K152443Vericore Gradient Temporary Disc K241729Hard Splint & Thermo-Adaptive Splint

Related Devices (Code: MQC)

K170985Urbanek DeviceTmj Services, LLC K161884Ortho System3Shape A/S K191836Ceramill A-SplintAmann Girrbach AG K183598KeyPrint KeySplint SoftKeystone Industries K182820The PODAdvanced Facialdontics, LLC K181361Brux Night GuardBrux Night Guard

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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