Vericore Abutment in Titanium for Implant Systems

FDA 510(k) K092857 · Whip-Mix Corp.

Substantially Equivalent

510(k) numberK092857

Submission

Device name
Vericore Abutment in Titanium for Implant Systems
Applicant
Whip-Mix Corp.
Louisville, KY, US
Received
September 16, 2009
Decision date
March 4, 2010
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
NHA – Abutment, Implant, Dental, Endosseous
Device class
Class II (moderate risk)
Regulation
21 CFR 872.3630
Specialty
Dental
Implant
Yes

To be used in conjunction with an endosseous dental implant fixture to aid in prosthetic rehabilitation.

Other 510(k)s with product code NHA

510(k)DeviceApplicantDecision
K253999Universal Base ASC Engaging; Universal Base ASC Non-Engaging; Universal Base MUA ASC…NHA · Traditional Nobel Biocare AB08/06/2026SE
K261147Neodent Implant System - NeoConvert FitNHA · Traditional JJGC Indústria e Comércio de Materiais Dentários…07/01/2026SE
K261122Mist IcNHA · Traditional Imagine Milling Technologies, LLC06/27/2026SE
K260061BioHorizons CEREC Compatible Ti-BasesNHA · Traditional BioHorizons Implant Systems, Inc.06/26/2026SE
K253922Neodent Scannable Healing AbutmentNHA · Traditional JJGC Indústria e Comércio de Materiais Dentários…06/15/2026SE
K254145Omni-Directional Multi-Unit Abutment System (Trade Name: Omnibut™)NHA · Abbreviated Smart Denture Conversions, LLC06/11/2026SE
K260564DESS Dental Smart SolutionsNHA · Traditional Terrats Medical SL06/09/2026SE
K252904SIC Abutments including CAD/CAM SolutionsNHA · Traditional Sic Invent AG06/03/2026SE
K253774Elos Accurate® Denture Fixation SystemNHA · Traditional Elos Medtech Pinol A/S05/20/2026SE
K253372ET Healing Abutments; ET Scan Healing Abutments; EK Scan Healing AbutmentsNHA · Traditional Hiossen, Inc.05/14/2026SE

More from Hiossen, Inc.

510(k)DeviceDecision
K241729Hard Splint & Thermo-Adaptive SplintMQC · Traditional 03/18/2025SE
K190107VeriSplintMQC · Traditional 07/10/2019SE
K152443Vericore Gradient Temporary DiscEBG · Traditional 05/11/2016SE
K142670Vericore Zirconia BlanksEIH · Special 10/22/2014SE
K140877Vericore Zirconia BlanksEIH · Traditional 09/03/2014SE
K140146Comfortsoft Soft Denture Liner SystemEBI · Traditional 04/29/2014SE
K131760Whip Mix Preppies PlusEJR · Traditional 03/26/2014SE
K090976Vericore Abutment in Zirconia for Implant SystemsNHA · Traditional 06/25/2009SE
K082299Vericore Implant AbutmentsNHA · Traditional 11/20/2008SE

Questions and answers

When was Vericore Abutment in Titanium for Implant Systems cleared by the FDA?

Vericore Abutment in Titanium for Implant Systems (K092857) received a 510(k) decision of Substantially Equivalent on March 4, 2010, 169 days after the submission was received.

What is the product code of K092857?

The FDA product code is NHA – Abutment, Implant, Dental, Endosseous, a Class II (moderate risk) device regulated under 21 CFR 872.3630.