Manufacturer registered with FDA

Greater Curve

Cincinnati, OH, United States. Lists 2 dental device types with FDA across 1 registered establishment.

FDA owner/operator10082825Repacker / relabelerSpecification developer
Device types listed
2
Brands and models
14
510(k) clearances
0as applicant
Markets registered in
33 registrations outside the US
Establishments
1United States

Registered in 3 markets

Where regulators' registries name Greater Curve as the manufacturer or the registration holder of a device.

All markets
United States: 2 device types listedUnited Kingdom: 2 registrationsAustralia: 1 registrations
RegisteredHome: United StatesOne marker per market
MarketRegulatorNamed asName on the registryRegistrationsIssuedRecords
United StatesFDAManufacturerGreater Curve2 device types—Below
United KingdomMHRAManufacturerGreater Curve2—Pure Global AI
AustraliaTGAManufacturerGreater Curve12026–2026Pure Global AI

Outside the US the count is of all the company's device registrations in that market, dental or not · matched by company name and country · registry data read 12 Nov 2026

Devices listed with FDA

What Greater Curve currently lists, by FDA device type, with the brand and model names on the listing.

Device typeCategoryRoleBrands and modelsListed since
Operative Matrix Contouring InstrumentEKF · Class 1Dental hand instrumentsMaker
Greater Curve Large Brass Sectional MatrixGreater Curve Micro Thin matrix bandsGreater Curve Micro U-Band matrix bandsGreater Curve Micro Wide matrix bandsGreater Curve Small Brass Sectional MatrixGreater Curve Standard Brass matrix bandsGreater Curve Standard matrix bandsGreater Curve U-Band Brass matrix bandsGreater Curve U-Band matrix bandsGreater Curve Wide Brass matrix bands
1 more
Greater Curve Wide matrix bands
2021
Matrix RetainerJEP · Class 1Dental hand instrumentsLister
Greater Curve Saliva Ejector HolderGreater Curve Soft Sided Contra-angle RetainerGreater Curve Soft Sided Universal Retainer
2021

Source: FDA establishment registration & device listing, 510(k) and product classification files · FDA data as of 2 Nov 2026 · snapshot 12 Nov 2026

Registered establishments

EstablishmentLocationWhat it does
GREATER CURVEFDA reg. 3020650140Cincinnati, OH, United StatesRepacker / relabeler, Specification developer

Sources

FDA establishment registration & device listing (search FDA, owner/operator 10082825). FDA 510(k) premarket notification file. FDA data as of 2 Nov 2026; snapshot 12 Nov 2026. The location shown is the address on FDA's record.