Manufacturer registered with FDA
DTE Oregon, Inc
Bay Minette, AL, United States. Lists 3 dental device types with FDA across 1 registered establishment.
- Device types listed
- 3
- Brands and models
- 5
- 510(k) clearances
- 0as applicant
- Markets registered in
- 215 registrations outside the US
- Establishments
- 1United States
Registered in 2 markets
Where regulators' registries name DTE Oregon, Inc 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 | DTE Oregon, Inc | 3 device types | — | Below |
| Canada | Health Canada | Registration holder | DTE OREGON, INC. | 15 | 2007–2007 | 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 DTE Oregon, Inc currently lists, by FDA device type, with the brand and model names on the listing.
| Device type | Category | Role | Brands and models | Listed since |
|---|---|---|---|---|
| Dental Operating LightEAZ · Class 1 | Dental operating lights | Maker | 9040 Operatory Light, 9070, Dental Operatory Light, 9080 Dental Operatory Light | 2019 |
| Operative Dental UnitEIA · Class 1 | Dental chairs & operative units | Maker | Forest Dental Delivery System, LSM and Elite Unit | 2019 |
| Dental Chair without Operative UnitNRU · Class 1 | Dental chairs & operative units | Maker | 3800 Operatory Chair3900 Operatory Chair6400 Operatory Chair | 2019 |
Source: FDA establishment registration & device listing, 510(k) and product classification files · FDA data as of 2 Nov 2026 · snapshot 12 Nov 2026
Also lists devices cleared under other names
DTE Oregon, Inc lists these devices with FDA today. The clearance names a different applicant, as happens after a rename, an acquisition or a private-label agreement.
Original applicants: Forest Dental Products, Inc. (1).
| Decided | 510(k) | Device | Applicant | Device type |
|---|---|---|---|---|
| 17 Aug 2018 | K173608 | Forest Dental Unit | Forest Dental Products, Inc. | EIA Operative Dental Unit |
Registered establishments
| Establishment | Location | What it does |
|---|---|---|
| FOREST DENTAL EQUIPMENTFDA reg. 3022226 | Bay Minette, AL, United States | Contract manufacturer, Manufacturer, Remanufacturer, Repacker / relabeler |
Other names on FDA records
Forest Dental Equipment
Sources
FDA establishment registration & device listing (search FDA, owner/operator 10059617). 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.