Manufacturer registered with FDA
Beaverstate Dental, Inc.
Newberg, OR, United States. Lists 6 dental device types with FDA across 1 registered establishment, and holds 2 510(k) clearances as applicant.
- Device types listed
- 6
- Brands and models
- 94
- 510(k) clearances
- 21995–1995
- Markets registered in
- 1United States
- Establishments
- 1United States
510(k) clearances per year, 1990–2026
Devices listed with FDA
What Beaverstate Dental, 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 |
|---|---|---|---|---|
| Saliva Ejector MouthpieceDYN · Class 1 | — | Maker | 112-262 HVE VALVE STANDARD112-263 HVE VALVE UNIVERSAL112-280 SALIVA EJECTOR VALVE | 2017 |
| Dental Operating LightEAZ · Class 1 | Dental operating lights | Maker | CLX-110CLX-220FL-3000 | 2017 |
| Suction Operatory UnitEBR · Class 1 | Suction & evacuation units | Maker | A-4550A-5000A-5032A-5124A-5132A-5150A-5200A-5210A-5221A-5222 4 moreA-5230A-5524H-5200S-5225 | 2017 |
| Air and/or Water Syringe UnitECB · Class 1 | Dental hand instruments | Maker | 113-014113-015113-202113-400113-505113-508113-510113-513113-514113-515 | 1992 |
| Operative Dental UnitEIA · Class 1 | Dental chairs & operative units | Maker | A-050A-100A-101A-200A-202A-220A-222A-230A-250A-300 53 moreA-3100A-3101A-3103A-3150A-3151A-3153A-400A-4100A-4150H-3600PM-200PM-220PM-400PM-4500PM-4501PM-4550PM-4551RD-3101RD-3102RD-3103RD-3150RD-3151RD-3152RD-3153RD-4250RD-4600RD-4650S-2500S-2506S-330S-3300S-3306S-3420S-3426S-3600S-3606S-3620S-3621S-3630S-3636S-4100S-4150S-4250S-4300S-4350S-5325S-6300S-6307SC-4200SC-4250SD-3302SO-3304SO-3354 | 2019 |
| Dental Chair without Operative UnitNRU · Class 1 | Dental chairs & operative units | Maker | EPIC | 2017 |
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 |
|---|---|---|
| BEAVERSTATE DENTAL, INC.FDA reg. 3019103 | NEWBERG, OR, United States | Manufacturer, Repacker / relabeler |
Sources
FDA establishment registration & device listing (search FDA, owner/operator 3019103). 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.