Registered with FDA
BFW, Inc.
Rapid City, SD, United States. Lists 1 dental device type with FDA across 1 registered establishment.
- Device types listed
- 1
- Brands and models
- 1
- 510(k) clearances
- 0as applicant
- Markets registered in
- 35 registrations outside the US
- Establishments
- 1United States
Registered in 3 markets
Where regulators' registries name BFW, 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 | Lister | BFW, Inc. | 1 device types | — | Below |
| Taiwan | TFDA | Manufacturer | BFW, INC. | 4 | 2005–2006 | Pure Global AI |
| Israel | AMAR | Manufacturer | BFW Inc | 1 | — | 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 BFW, 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 |
|---|---|---|---|---|
| Surgical Headlight LightEBA · Class 1 | Dental operating lights | Lister | KITSILANO LED Headlight | 2025 |
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 |
|---|---|---|
| BFW, INC.FDA reg. 3005775121 | Rapid City, SD, United States | Repacker / relabeler |
Sources
FDA establishment registration & device listing (search FDA, owner/operator 10027296). 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.