Manufacturer registered with FDA

Jieyang Top-Tip'S Daily Use Products Co.,ltd.

JIEYANG, China. Lists 1 dental device type with FDA across 1 registered establishment.

FDA owner/operator10046665Manufacturer
Device types listed
1
Brands and models
1
510(k) clearances
0as applicant
Markets registered in
317 registrations outside the US
Establishments
1China

Registered in 3 markets

Where regulators' registries name Jieyang Top-Tip'S Daily Use Products Co.,ltd. as the manufacturer or the registration holder of a device.

All markets
United States: 1 device types listedPeru: 9 registrationsColombia: 8 registrations
RegisteredHome: ChinaOne marker per market
MarketRegulatorNamed asName on the registryRegistrationsIssuedRecords
United StatesFDAManufacturerJieyang Top-Tip'S Daily Use Products Co.,ltd.1 device types—Below
PeruDIGEMIDManufacturerJIEYANG TOP-TIP´S DAILY USE PRODUCTS CO., LTD.JIEYANG TOP TIP´S DAILY USE PRODUCTS CO., LTD.92013–2016Pure Global AI
ColombiaINVIMAManufacturerJIEYANG TOP-TIP'S DAILY USE PRODUCTS CO., LTDA.JIEYANG TOP-TIP’S DAILY USE PRODUCTS CO.,LTD · JIEYANG TOP-TIP'S DAILY USE PRODUCTS CO., LTD8—Pure 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 Jieyang Top-Tip'S Daily Use Products Co.,ltd. currently lists, by FDA device type, with the brand and model names on the listing.

Device typeCategoryRoleBrands and modelsListed since
Roll CottonEFN · Class 1—Maker
COTTON, ROLL
2014

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
JIEYANG TOP-TIP'S DAILY USE PRODUCTS CO.,LTD.FDA reg. 3004595864JIEYANG Guangdong, ChinaManufacturer

Sources

FDA establishment registration & device listing (search FDA, owner/operator 10046665). 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.