Manufacturer registered with FDA

Mipont Medical Equipment Co., Ltd.

guangzhou, China. Lists 2 dental device types with FDA across 1 registered establishment, and holds 1 510(k) clearance as applicant.

FDA owner/operator10094205Manufacturer1 clearance in five years
Device types listed
2
Brands and models
2
510(k) clearances
12025–2025
Markets registered in
1United States
Establishments
1China
2025: 120102020

510(k) clearances per year, 2007–2026

Devices listed with FDA

What Mipont Medical Equipment Co., Ltd. currently lists, by FDA device type, with the brand and model names on the listing.

Device typeCategoryRoleBrands and modelsListed since
Operative Dental UnitEIA · Class 1Dental chairs & operative unitsMaker
Integral Dental Units
2025
Dental Chair with Operative UnitKLC · Class 1Dental chairs & operative unitsMaker
Integral Dental Units
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 Mipont Medical Equipment Co., Ltd. as the applicant.

Decided510(k)DeviceDevice type
27 May 2025K242611Integral Dental UnitsEIA Operative Dental Unit

Registered establishments

EstablishmentLocationWhat it does
MIPONT MEDICAL EQUIPMENT CO., LTD.FDA reg. 3042256511guangzhou Guangdong, ChinaManufacturer

Sources

FDA establishment registration & device listing (search FDA, owner/operator 10094205). 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.