Manufacturer registered with FDA
Bailey Instruments Ltd
Manchester, United Kingdom. Lists 2 dental device types with FDA across 1 registered establishment.
- Device types listed
- 2
- Brands and models
- 0
- 510(k) clearances
- 0as applicant
- Markets registered in
- 587 registrations outside the US
- Establishments
- 1United Kingdom
Registered in 5 markets
Where regulators' registries name Bailey Instruments Ltd 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 | Bailey Instruments Ltd | 2 device types | — | Below |
| United Kingdom | MHRA | Manufacturer | Bailey Instruments Ltd | 71 | — | Pure Global AI |
| European Union | EUDAMED | Manufacturer | Bailey Instruments Ltd | 7 | — | Pure Global AI |
| Saudi Arabia | SFDA | Manufacturer | Bailey Instruments Ltd | 6 | — | Pure Global AI |
| Australia | TGA | Manufacturer | Bailey Instruments Ltd | 3 | 2004–2012 | 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 Bailey Instruments Ltd 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 Instrument HandleEJB · Class 1 | Dental hand instruments | Maker | — | 2002 |
| Cartridge SyringeEJI · Class 2 | Dental needles & syringes | Maker | — | 2023 |
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 |
|---|---|---|
| Bailey Instruments LtdFDA reg. 3001084743 | Manchester, United Kingdom | Manufacturer |
Sources
FDA establishment registration & device listing (search FDA, owner/operator 9033619). 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.