FDA 510(k)

VeriSplint

K-Number: K190107 · 2019-07-10

Decision Date2019-07-10

Product CodeMQC

DecisionSubstantially Equivalent

Device Summary

VeriSplint is the device name listed in this FDA 510(k) record. The listed applicant is Whip Mix Corporation. It received FDA 510(k) clearance on 2019-07-10 under 510(k) 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. The listed applicant is Whip Mix Corporation. The 510(k) number is K190107.

When did VeriSplint receive FDA 510(k) clearance?

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

Who is the listed applicant for VeriSplint?

The FDA 510(k) record lists Whip Mix Corporation as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VeriSplint?

The FDA product code for VeriSplint is MQC.

Other records listing Whip Mix Corporation as applicant

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.

K241729Hard Splint & Thermo-Adaptive Splint K152443Vericore Gradient Temporary Disc

Related Devices (Code: MQC)

K253798UltraPrint-Dental Hard Splint UVGuangzhou Heygears IMC., Inc.K250743Remvia NightGuardRemvia K251252NOBILCAM IMPAK DiscShandong Huge Dental Material Corporation K241729Hard Splint & Thermo-Adaptive SplintWhip Mix Corporation K243516Remi Custom Night GuardGrindguard, Inc.K241369LIJIA Night GuardLijia, LLC

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.