Manufacturer registered with FDA

Quickdent Devices Private Limited

Mumbai, India. Lists 4 dental device types with FDA across 1 registered establishment, and holds 1 510(k) clearance as applicant.

FDA owner/operator10092670Repacker / relabelerSpecification developer1 clearance in five years
Device types listed
4
Brands and models
3
510(k) clearances
12024–2024
Markets registered in
23 registrations outside the US
Establishments
1India
2024: 120102020

510(k) clearances per year, 2007–2026

Registered in 2 markets

Where regulators' registries name Quickdent Devices Private Limited as the manufacturer or the registration holder of a device.

All markets
United States: 4 device types listedIndia: 3 registrations
RegisteredHome: IndiaOne marker per market
MarketRegulatorNamed asName on the registryRegistrationsIssuedRecords
United StatesFDAManufacturerQuickdent Devices Private Limited1 clearances2024–2024Below
IndiaCDSCORegistration holderQuickdent Devices Private Limited32022–2022Pure 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 Quickdent Devices Private Limited currently lists, by FDA device type, with the brand and model names on the listing.

Device typeCategoryRoleBrands and modelsListed since
Root-Form Endosseous ImplantDZE · Class 2Dental implantsMaker
Quickdent Dental Implant System
2025
Endosseous Dental Implant AccessoriesNDP · Class 1Implant instruments & surgical kitsMaker
Quickdent dental implant accessories
2025
Endosseous Dental Implant AbutmentNHA · Class 2Implant abutmentsMaker
Quickdent Dental Implant System
2025
Non-Irrigation Endosseous Dental Implant Drill BitsQRQ · Class 1Implant instruments & surgical kitsLister—2025

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

510(k) clearances

Clearances on which FDA names Quickdent Devices Private Limited as the applicant.

Decided510(k)DeviceDevice type
19 Dec 2024K243094Quickdent Dental Implant SystemDZE Root-Form Endosseous Implant

Registered establishments

EstablishmentLocationWhat it does
QUICKDENT DEVICES PRIVATE LIMITEDFDA reg. 3036779616Mumbai Maharashtra, IndiaRepacker / relabeler, Specification developer

Sources

FDA establishment registration & device listing (search FDA, owner/operator 10092670). 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.