Manufacturer registered with FDA

Dreame Technology Usa Inc.

Lewes, DE, United States. Lists 4 dental device types with FDA across 1 registered establishment.

FDA owner/operator10096203Repacker / relabelerSpecification developer
Device types listed
4
Brands and models
27
510(k) clearances
0as applicant
Markets registered in
1United States
Establishments
1United States

Devices listed with FDA

What Dreame Technology Usa Inc. 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
T01 Portable Water FlosserT02 Pro UV Portabal Water FlosserWT10 Water Flosser
2026
Manual ToothbrushEFW · Class 1ToothbrushesMaker
EH10 Gentle Care Brush HeadEH11 Deep Clean Brush HeadFH01 Full-clean brush headFH02 Full-clean brush headXH01 Xpert Clean Brush headXH02 Xpert Clean Brush headXH03 Xpert Gentle Brush headXH04 Xpert Gentle Brush headXH07 Xpert Clean Brush headXH08 Xpert Clean Brush head
2 more
XH09 Xpert Gentle Brush headXH10 Xpert Gentle Brush head
2026
Powered ToothbrushJEQ · Class 1ToothbrushesMaker
E10F Sonic Vibration Electric ToothbrushE10S Sonic Vibration Electric ToothbrushF01 Soinc Electric ToothbrushF02 Pro Sonic & Vibration Electric ToothbrushF02 Sonic & Vibration Electric ToothbrushF03 Pro Electric ToothbrushNB01 Smart Sonic Electric ToothbrushX10 Pro Electric ToothbrushX10F Electric Toothbrush
2026
Dental FlossJES · Class 1Floss & interdental cleanersMaker
DF01 Pro Strong Mint Twin Line Dental Floss PicksDF01 Strong Mint Twin Line Dental Floss PicksDF02 Strong Mint Twin Line Dental Floss Picks
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
DREAME TECHNOLOGY USA INCFDA reg. 3046158144Newark, DE, United StatesRepacker / relabeler, Specification developer

Sources

FDA establishment registration & device listing (search FDA, owner/operator 10096203). 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.