Manufacturer registered with FDA

Jiangyin Jintaike Biotech Co., Ltd.

Jiangyin, China. Lists 4 dental device types with FDA across 1 registered establishment.

FDA owner/operator10044800Manufacturer
Device types listed
4
Brands and models
4
510(k) clearances
0as applicant
Markets registered in
21 registrations outside the US
Establishments
1China

Registered in 2 markets

Where regulators' registries name Jiangyin Jintaike Biotech Co., Ltd. as the manufacturer or the registration holder of a device.

All markets
United States: 4 device types listedTaiwan: 1 registrations
RegisteredHome: ChinaOne marker per market
MarketRegulatorNamed asName on the registryRegistrationsIssuedRecords
United StatesFDAManufacturerJiangyin Jintaike Biotech Co., Ltd.4 device types—Below
TaiwanTFDAManufacturerJIANGYIN JINTAIKE BIOTECH CO., LTD12016–2016Pure 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 Jiangyin Jintaike Biotech Co., Ltd. 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
DRILL, DENTAL, INTRAORAL
2014
Dental Hand InstrumentsDZN · Class 1Dental hand instrumentsMaker
INSTRUMENTS, DENTAL HAND
2014
Backing and Facing Artificial TeethELK · Class 1—Maker
TEETH, ARTIFICIAL, BACKING AND FACING
2013
Endosseous Dental Implant AccessoriesNDP · Class 1Implant instruments & surgical kitsMaker
Accessories, implant, dental, endosseous
2013

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
JINTAIK (Yunnan) BIOTECH CO., LTD.FDA reg. 3010453282Kunming Yunnan, ChinaManufacturer

Other names on FDA records

JINTAIK (Yunnan) BIOTECH CO., LTD.

Sources

FDA establishment registration & device listing (search FDA, owner/operator 10044800). 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.