Manufacturer registered with FDA
QSA Surgical
SIALKOT, Pakistan. Lists 14 dental device types with FDA across 2 registered establishments.
- Device types listed
- 14
- Brands and models
- 5
- 510(k) clearances
- 0as applicant
- Markets registered in
- 4411 registrations outside the US
- Establishments
- 2United Arab Emirates, Pakistan
Registered in 4 markets
Where regulators' registries name QSA Surgical 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 | QSA Surgical | 14 device types | — | Below |
| Thailand | Thai FDA | Manufacturer | QSA SURGICAL (PVT) LTD | 353 | — | Pure Global AI |
| South Korea | MFDS | Manufacturer | QSA SURGICAL PVT LTD.ULTIMATE MEDICAL PRODUCTS LTD · QSA SURGICAL (PVT) LTD. · +2 | 51 | 2006–2025 | Pure Global AI |
| Taiwan | TFDA | Manufacturer | QSA SURGICAL PRIVATE LIMITEDULTIMATE MEDICAL PRODUCTS LTD. · QSA SURGICAL (PVT) LTD | 7 | 2006–2020 | 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 QSA Surgical 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 |
|---|---|---|
| QSA SURGICAL (PVT) LTD.FDA reg. 8040233 | SIALKOT Punjab, Pakistan | Contract manufacturer |
| ULTIMATE MEDICAL PRODUCTS LTD.FDA reg. 9710524 | SHARJAH Ash Shariqah, United Arab Emirates | Foreign exporter |
Other names on FDA records
Ultimate Medical Products Ltd.
Sources
FDA establishment registration & device listing (search FDA, owner/operator 8040233). 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.