Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3020650140

FEI Number

3020650140

Entity Name

GREATER CURVE

City/State/Country

Cincinnati, OH, US

Establishment Address

4030 Mt. Carmel-Tobasco Rd. Suite 314, Cincinnati, OH 45255, US

Establishment Type(s)

Repack or Relabel Medical Device,Develop Specifications But Do Not Manufacture At This Facility

Owner / Operator

Greater Curve (Owner Number: 10082825)

Owner / Operator Contact Address

4030 Mt. Carmel-Tobasco Rd. Suie 314, Cincinnati, OH 45255, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Greater Curve Soft Sided Universal Retainer Greater Curve Saliva Ejector Holder Greater Curve Soft Sided Contra-angle Retainer Greater Curve Micro Wide matrix bands Greater Curve Wide matrix bands Greater Curve U-Band matrix bands Greater Curve Wide Brass matrix bands Greater Curve Standard Brass matrix bands Greater Curve Micro Thin matrix bands Greater Curve Micro U-Band matrix bands Greater Curve Large Brass Sectional Matrix Greater Curve Standard matrix bands Greater Curve Small Brass Sectional Matrix Greater Curve U-Band Brass matrix bands

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
JEP	Retainer, Matrix	Dental	Class 1	872.4565	2021-10-06
EKF	Instrument, Contouring, Matrix, Operative	Dental	Class 1	872.4565	2021-10-06

Official Correspondent

Justine Muzzillo

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Greater Curve

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
K831136	Almore Intl., Inc.	DOUBLE BOW TOOTH SEPARATOR	1983-06-08

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3020650140. Last updated year: 2026. Please use registration number 3020650140 when referencing this establishment in official correspondence.