Data / Medical devices / United States / Forest Dental Equipment
Forest Dental Equipment: FDA-registered device maker in Bay Minette, AL, United States, 1 510(k) clearance
Forest Dental Equipment is registered with the FDA (registration 3022226) in Bay Minette, AL, United States. It lists 3 device types. The FDA files 1 510(k) clearance under its listings, the newest dated August 17, 2018. Registered through 2027. FDA data exported November 2, 2026.
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- FDA registration number
- 3022226
- Address
- 2500 US Highway 31, Bay Minette, AL, United States, 36507
- Owner or operator
- DTE Oregon, Inc (10059617)
- Roles
- Contract manufacturer, Manufacturer, Remanufacturer, Repackager or relabeler
- First device listed
- February 4, 2019
- Registered through
- 2027
- Brand names listed
- 3800 Operatory Chair, 3900 Operatory Chair, 6400 Operatory Chair, 9040 Operatory Light, 9070, Dental Operatory Light, 9080 Dental Operatory Light, Forest Dental Delivery System, LSM and Elite Unit
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Chair, Dental, Without Operative Unit | NRU | 1 | Remanufacturer, Repackager or relabeler | accessdata.fda.gov |
| Light, Operating, Dental | EAZ | 1 | Manufacturer, Repackager or relabeler | accessdata.fda.gov |
| Unit, Operative Dental | EIA | 1 | Contract manufacturer, Manufacturer | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| August 17, 2018 | K173608 | Forest Dental Unit | EIA | Substantially Equivalent | Forest Dental Products, Inc. | accessdata.fda.gov |
Compare with other makers
- All makers of Chair, Dental, Without Operative Unit
- All makers of Light, Operating, Dental
- All makers of Unit, Operative Dental
Updated August 17, 2018. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.