Manufacturer registered with FDA

Kazan Medical Instruments Plant

Kazan, Russia. Lists 7 dental device types with FDA across 1 registered establishment.

FDA owner/operator10060925Manufacturer
Device types listed
7
Brands and models
4
510(k) clearances
0as applicant
Markets registered in
27 registrations outside the US
Establishments
1Russia

Registered in 2 markets

Where regulators' registries name Kazan Medical Instruments Plant as the manufacturer or the registration holder of a device.

All markets
United States: 7 device types listedSouth Korea: 7 registrations
RegisteredHome: RussiaOne marker per market
MarketRegulatorNamed asName on the registryRegistrationsIssuedRecords
United StatesFDAManufacturerKazan Medical Instruments Plant7 device types—Below
South KoreaMFDSManufacturerKazan Medical Instruments Plant72016–2016Pure 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 Kazan Medical Instruments Plant currently lists, by FDA device type, with the brand and model names on the listing.

Device typeCategoryRoleBrands and modelsListed since
Intraoral Dental DrillDZA · Class 1Surgical drills & motorsMaker
Burs 11-018-5
2019
Dental Diamond InstrumentDZP · Class 1Dental burs & diamondsMaker
Diamond bur GSAP 2,3P-8C
2019
Dental BurEJL · Class 1Dental burs & diamondsMaker—2019
Endodontic Pulp Canal ReamerEKP · Class 1Endodontic filesMaker—2019
Endodontic Pulp Canal FileEKS · Class 1Endodontic filesMaker
H-file manual
2019
Endodontic BroachEKW · Class 1Endodontic filesMaker
Barbed broaches short L-30 mm
2019
Periodontic FileEMR · Class 1Dental hand instrumentsMaker—2019

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
KAZAN MEDICAL INSTRUMENTS PLANTFDA reg. 3012501675Kazan Tatarstan, RussiaManufacturer

Sources

FDA establishment registration & device listing (search FDA, owner/operator 10060925). 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.