Manufacturer registered with FDA
W.R. Rayson Co Inc
Burgaw, NC, United States. Lists 2 dental device types with FDA across 1 registered establishment.
- Device types listed
- 2
- Brands and models
- 2
- 510(k) clearances
- 0as applicant
- Markets registered in
- 34 registrations outside the US
- Establishments
- 1United States
Registered in 3 markets
Where regulators' registries name W.R. Rayson Co 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 | W.R. Rayson Co Inc | 2 device types | — | Below |
| Australia | TGA | Manufacturer | W.R. Rayson Co Inc | 2 | 2018–2018 | Pure Global AI |
| South Korea | MFDS | Manufacturer | W.R. RAYSONW.R. Rayson Co., Inc. | 2 | 2013–2015 | 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 W.R. Rayson Co 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 Hand InstrumentsDZN · Class 1 | Dental hand instruments | Maker | Mylar Matrix Strips | 2013 |
| Articulation PaperEFH · Class 1 | — | Maker | ARTICULATING PAPER | 2001 |
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 |
|---|---|---|
| W.R. RAYSON CO., INC.FDA reg. 2431400 | BURGAW, NC, United States | Manufacturer, Repacker / relabeler |
Sources
FDA establishment registration & device listing (search FDA, owner/operator 2431400). 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.