Manufacturer registered with FDA
Medisporex Private Limited
SIALKOT, PUNJAB, Pakistan. Lists 42 dental device types with FDA across 1 registered establishment.
- Device types listed
- 42
- Brands and models
- 46
- 510(k) clearances
- 0as applicant
- Markets registered in
- 81,072 registrations outside the US
- Establishments
- 1Pakistan
Registered in 8 markets
Where regulators' registries name Medisporex Private Limited 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 | Medisporex Private Limited | 42 device types | — | Below |
| Thailand | Thai FDA | Manufacturer | MEDISPOREX (PVT) LTD | 1,004 | — | Pure Global AI |
| Colombia | INVIMA | Registration holder | MEDISPOREX PRIVATE LIMITED | 31 | — | Pure Global AI |
| Brazil | ANVISA | Manufacturer | MEDISPOREX PRIVATE LIMITED.MEDISPOREX PVT LTD | 13 | 2008–2023 | Pure Global AI |
| Costa Rica | Ministerio de Salud | Manufacturer | MEDISPOREX (PVT) LTD. | 12 | — | Pure Global AI |
| South Korea | MFDS | Manufacturer | Medisporex(Pvt.) Ltd.Medisporex (Pvt) Ltd. · Medisporex (Pvt.) Ltd. | 10 | 2000–2001 | Pure Global AI |
| Australia | TGA | Manufacturer | Medisporex Private Limited | 1 | 2025–2025 | Pure Global AI |
| Taiwan | TFDA | Manufacturer | MEDISPOREX(PVT)LTD., | 1 | 2012–2012 | 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 Medisporex Private Limited currently lists, by FDA device type, with the brand and model names on the listing.
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 |
|---|---|---|
| MEDISPOREX (PVT) LTD.FDA reg. 8040881 | SIALKOT Punjab, Pakistan | Contract manufacturer, Manufacturer |
Sources
FDA establishment registration & device listing (search FDA, owner/operator 8040881). 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.