ABRASIVE TECHNOLOGY, LLC

FDA Device Registration & Listing · LEWIS CENTER, OH, US · Registration 1525838

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
1525838
FEI Number
1525838
Entity Name
ABRASIVE TECHNOLOGY, LLC
City/State/Country
LEWIS CENTER, OH, US
Establishment Address
8400 Green Meadows Drive N., LEWIS CENTER, OH 43035, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
ABRASIVE TECHNOLOGY, LLC (Owner Number: 1525838)
Owner / Operator Contact Address
8400 Green Meadows Drive N., --, Lewis Center, OH 43035, US
Initial Importer Flag
Y
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

APPLICATORS MANDRELS STAINBUSTER PRODIA Two Striper Prodia Priva Prodia Sport LUMINESCENCE PLUS LUMINESCENCE INTRAORAL DRILL CARBOPOST, SNOWPOST, SNOWLIGHT CARBOPOST SNOWLIGHT SNOWPOST Two Striper Diamond Finishing Strips COMPO-STRIP

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
EHK Cup, Prophylaxis Dental Class 1 872.6290 2002-08-21
EHJ Disk, Abrasive Dental Class 1 872.6010 2002-08-21
EHL Point, Abrasive Dental Class 1 872.6010 2006-02-23
DZP Instrument, Diamond, Dental Dental Class 1 872.4535 1992-11-22
EJR Agent, Polishing, Abrasive, Oral Cavity Dental Class 1 872.6030 2002-08-21
GFF Bur, Surgical, General & Plastic Surgery General, Plastic Surgery Class 1 878.4820 2002-08-21
DZA Drill, Dental, Intraoral Dental Class 1 872.4130 2006-02-23
ELR Post, Root Canal Dental Class 1 872.3810 2006-02-23
EHM Strip, Polishing Agent Dental Class 1 872.6010 1992-11-22

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

ABRASIVE TECHNOLOGY, LLC
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K121698 Dentsply International, Inc. NUPRO SENSODYNE PROPHYLAXIS PASTE WITH NOVAMIN 2012-08-06

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 1525838. Last updated year: 2026. Please use registration number 1525838 when referencing this establishment in official correspondence.
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