Manufacturer registered with FDA
Dr. Brown's Company
Saint Louis, MO, United States. Lists 4 dental device types with FDA across 2 registered establishments.
- Device types listed
- 4
- Brands and models
- 4
- 510(k) clearances
- 0as applicant
- Markets registered in
- 33 registrations outside the US
- Establishments
- 2United States
Registered in 3 markets
Where regulators' registries name Dr. Brown's Company as the manufacturer or the registration holder of a device.
| Market | Regulator | Named as | Name on the registry | Registrations | Issued | Records |
|---|---|---|---|---|---|---|
| United States | FDA | Manufacturer | Dr. Brown's Company | 4 device types | — | Below |
| Colombia | INVIMA | Manufacturer | DR. BROWN'S COMPANY | 2 | — | Pure Global AI |
| Canada | Health Canada | Registration holder | DR. BROWN'S COMPANY | 1 | 2021–2021 | Pure 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 Dr. Brown's Company currently lists, by FDA device type, with the brand and model names on the listing.
| Device type | Category | Role | Brands and models | Listed since |
|---|---|---|---|---|
| Manual ToothbrushEFW · Class 1 | Toothbrushes | Maker | Dr. Brown's | 2014 |
| Powered ToothbrushJEQ · Class 1 | Toothbrushes | Maker | Dr. Brown's powered toothbrush | 2025 |
| Fluid-Filled Teething RingKKO · Class 2 | — | Maker | Dr. Browns | 2024 |
| Teething Ring Non-Fluid FilledMEF · Class 1 | — | Maker | Dr. Brown's | 2014 |
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
| Establishment | Location | What it does |
|---|---|---|
| Dr. Brown's CompanyFDA reg. 3008138005 | Saint Louis, MO, United States | Specification developer |
| Dr. Brown's CompanyFDA reg. 3008819945 | Bonne Terre, MO, United States | Repacker / relabeler |
Sources
FDA establishment registration & device listing (search FDA, owner/operator 10033683). 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.