Manufacturer registered with FDA

Magenta Technology International Limited

Shenzhen, China. Lists 7 dental device types with FDA across 1 registered establishment.

FDA owner/operator10084167Contract manufacturerForeign exporterManufacturer
Device types listed
7
Brands and models
8
510(k) clearances
0as applicant
Markets registered in
1United States
Establishments
1China

Devices listed with FDA

What Magenta Technology International Limited currently lists, by FDA device type, with the brand and model names on the listing.

Device typeCategoryRoleBrands and modelsListed since
Heat Source for Bleaching TeethEEG · Class 1Teeth whitening lightsMaker
Teeth Whitening kitsTeeth Whitening Kits, whitening strips
2022
Manual ToothbrushEFW · Class 1ToothbrushesMaker
Toothpaste
2022
Irrigating (Dental) SyringeEIB · Class 1Dental hand instrumentsMaker
Water Flosser; Dental Irrigator(XY10, TC01, TC03, TC05, L13, KX685, AOW04, AOW04PRO)
2022
Dental Instrument HandleEJB · Class 1Dental hand instrumentsMaker
Stainless Dental Tools (Tonge Scraper, Dental Tweezers, Dental Mirror), Stainless Acne Needle Kit
2022
Periodontic ScalerEMN · Class 1Dental hand instrumentsMaker
Electric Teeth Cleaner (YJK031,YJK015A, L156, 161X, 701), Dental Denture Cleaner
2022
Powered ToothbrushJEQ · Class 1ToothbrushesMaker
Electric Toothbrush (K12, K1, K2, K3,F1, TB01N, TB-02N, TB-03N, TB-04, TB-05N, TB-06, TB-07N); U-shaped Tooth Brush Head
2022
Dental FlossJES · Class 1Floss & interdental cleanersMaker
Orthodontic Toothbrush, Interdental toothbrush, Supper Floss, Waxed Dental Floss, Orthodontic accessories
2025

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 Meijiante Technology Co., LtdFDA reg. 3021963363Shenzhen Guangdong, ChinaContract manufacturer, Foreign exporter, Manufacturer

Other names on FDA records

Shenzhen Meijiante Technology Co., Ltd

Sources

FDA establishment registration & device listing (search FDA, owner/operator 10084167). 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.