Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

Vericore Gradient Temporary Disc

K-Number: K152443 · 2016-05-11

ApplicantWhip Mix Corporation
Decision Date2016-05-11
Product CodeEBG
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

Vericore Gradient Temporary Disc 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 2016-05-11 under 510(k) number K152443. The device is classified under product code EBG. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Vericore Gradient Temporary Disc?

Vericore Gradient Temporary Disc is a medical device that received FDA 510(k) clearance on 2016-05-11. The listed applicant is Whip Mix Corporation. The 510(k) number is K152443.

When did Vericore Gradient Temporary Disc receive FDA 510(k) clearance?

Vericore Gradient Temporary Disc received FDA 510(k) clearance on 2016-05-11, under 510(k) number K152443.

Who is the listed applicant for Vericore Gradient Temporary Disc?

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 Vericore Gradient Temporary Disc?

The FDA product code for Vericore Gradient Temporary Disc is EBG.

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 SplintK190107VeriSplint

Related Devices (Code: EBG)

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.

K261261Dura-ArchHangzhou SHINING3D Dental Technology Co., Ltd.K253380“FLNT Base” and “FLNT Temp”Liaoning Upcera Co., Ltd.K251271TempFIT Temporary Crown and Bridge ResinRizhao Huge Biomaterials Company, Ltd.K243370DentaTOOTHAsiga Pty, Ltd.K243621Evoblock, PerléonEvoden Indústria Comércio Importação E ExportaçãoK243951TEMP MASTER, PMMA-based dental resinTaiwan Dental Materials Co., Ltd.

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.

↑