Manufacturer registered with FDA

Shenzhen Mericonn Technology Co., Ltd.

Shenzhen, China. Lists 2 dental device types with FDA across 1 registered establishment.

FDA owner/operator10062622Manufacturer
Device types listed
2
Brands and models
2
510(k) clearances
0as applicant
Markets registered in
43 registrations outside the US
Establishments
1China

Registered in 4 markets

Where regulators' registries name Shenzhen Mericonn Technology Co., Ltd. as the manufacturer or the registration holder of a device.

All markets
United States: 2 device types listedBrazil: 1 registrationsEuropean Union: 1 registrationsSouth Korea: 1 registrations
RegisteredHome: ChinaOne marker per market
MarketRegulatorNamed asName on the registryRegistrationsIssuedRecords
United StatesFDAManufacturerShenzhen Mericonn Technology Co., Ltd.2 device types—Below
BrazilANVISAManufacturerSHENZHEN MERICONN TECHNOLOGY CO.,LTD12023–2023Pure Global AI
European UnionEUDAMEDManufacturerShenzhen Mericonn Technology Co., Ltd1—Pure Global AI
South KoreaMFDSManufacturerShenzhen Mericonn Technology Co., Ltd12025–2025Pure 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 Shenzhen Mericonn Technology Co., Ltd. currently lists, by FDA device type, with the brand and model names on the listing.

Device typeCategoryRoleBrands and modelsListed since
Oral Irrigation UnitEFS · Class 1Oral irrigatorsMaker
Water flosser (model: YF9506, FP10, SK-D, JC-D, JC-D1, SK-D2, JC-D2)
2020
Powered ToothbrushJEQ · Class 1ToothbrushesMaker
Electric toothbrush (model: TB-1201, TB-1202, TB-1203, TB-1206)
2026

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
Shenzhen Mericonn Technology Co., Ltd.FDA reg. 3016595616Shenzhen Guangdong, ChinaManufacturer

Sources

FDA establishment registration & device listing (search FDA, owner/operator 10062622). 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.