Dreame Technology USA Inc (specification developer, Newark, DE): 4 new FDA device listings, incl. floss, dental

Dreame Technology USA Inc (Newark, Delaware): 4 new FDA device listings, incl. floss, dental. Its amount of 4 is above the median of 1 (83rd percentile). Dated 105 days ago, it serves as a historical benchmark. Score 70/100. As of 2026-10-28, from openFDA device registration and listing endpoint (U.S. Food and Drug Administration).

Data as of · Compiled by Zalwin from openFDA device registration and listing endpoint (U.S. Food and Drug Administration)

amount: 4 · 83th percentile of 2,570 DeviceEstablishmentPulse records · 4.0x the median

Free preview: all 14 published fields of this record are shown below. Locked: 36 related DE DeviceEstablishmentPulse records and the 5-column CSV export.

FieldValue
EstablishmentDreame Technology USA Inc
RoleSpecification developer (outsources manufacturing)
Establishment typesRepack or Relabel Medical Device; Develop Specifications But Do Not Manufacture At This Facility
LocationNewark, DE, US
New listings4
DevicesFloss, Dental; Toothbrush, Powered; Unit, Oral Irrigation; Toothbrush, Manual
Product codesJES, JEQ, EFS, EFW
Device classesClass I
Medical specialtiesDental
Brand namesDF01 Strong Mint Twin Line Dental Floss Picks; DF02 Strong Mint Twin Line Dental Floss Picks; DF01 Pro Strong Mint Twin Line Dental Floss Picks; E10S Sonic Vibration Electric Toothbrush; NB01 Smart Sonic Electric Toothbrush; F02 Sonic & Vibration Electric Toothbrush; X10 Pro Electric Toothbrush; F03 Pro Electric Toothbrush
First new listing2026-07-23
Latest new listing2026-07-23
FDA registration number3046158144
Registration expires2026-12-31
amount percentile83th of 2,570 (median 1, 4.0x median)
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CSV columns: Establishment · Role · New listings · Devices · Latest listing · official source URL

  • Source agency: openFDA device registration and listing endpoint (U.S. Food and Drug Administration)
  • Record date: 2026-07-23
  • Data refreshed: 2026-10-28
  • Refunds on request within 14 days

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LIVE PUBLIC DATA Source: openFDA device registration and listing endpoint (U.S. Food and Drug Administration) · Last refreshed: Wed, 28 Oct 2026 20:51:27 GMT

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Peer benchmark and outreach value: Dreame Technology USA Inc and 37 Delaware peers

  • Delaware DeviceEstablishmentPulse records like this one: 37
  • Dreame Technology USA Inc's amount: 83rd percentile of 2,570 records
  • Timing: Low: older than 30 days
  • Estimated pipeline if you contact every Delaware peer: $7,400 (peers × rate × deal size; an estimate from your assumptions, not a forecast)

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70 / 100 Score

  • Brings its own devices to market: buys manufacturing, sterilization and QMS help.
  • Several new listings at once.
  • U.S. establishment.

What is the DeviceEstablishmentPulse record for Dreame Technology USA Inc in Newark, Delaware?

Dreame Technology USA Inc (Newark, DE), a specification developer (outsources manufacturing), added 4 FDA device listings on 2026-07-23.

How does Dreame Technology USA Inc compare to other Delaware DeviceEstablishmentPulse records?

Its amount of 4 sits in the upper half (83th percentile) of 2,570 records; the median is 1. It is 105 days old; check the official source for later updates before acting. Its Score of 70/100 puts it among the stronger signals in this feed.

Dreame Technology USA Inc vs. top 3 peers

OrganizationLocationAmountPercentileRecord date
Dreame Technology USA IncNewark, DE483rd2026-07-23
Alc Enterprises IncBrooklyn, NY483rd2026-10-18
Deka Research & Development Corp.Manchester, NH483rd2026-09-25
Davol Inc., Sub. C.R. Bard, Inc.Warwick, RI377th2026-10-14

Related records

DeviceEstablishmentPulse: Specification developer (outsources manufacturing) DeviceEstablishmentPulse: U.S. establishment DeviceEstablishmentPulse: records in Delaware

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From the openFDA device registration and listing data, refreshed weekly. A listing shows a device an establishment says it makes or handles for the U.S. market; it is not FDA clearance or approval. Contact persons and street addresses are not stored. Verify in the FDA Establishment Registration and Device Listing database.

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