Manufacturer registered with FDA
Intersurgical UAB
PABRADE, Lithuania. Lists 1 dental device type with FDA across 1 registered establishment.
- Device types listed
- 1
- Brands and models
- 0
- 510(k) clearances
- 0as applicant
- Markets registered in
- 6108 registrations outside the US
- Establishments
- 1Lithuania
Registered in 6 markets
Where regulators' registries name Intersurgical UAB 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 | Intersurgical UAB | 1 device types | — | Below |
| Colombia | INVIMA | Manufacturer | UAB INTERSURGICALINTERSURGICAL UAB | 60 | — | Pure Global AI |
| South Korea | MFDS | Manufacturer | UAB IntersurgicalIntersurgical UAB | 23 | 2003–2026 | Pure Global AI |
| Taiwan | TFDA | Manufacturer | UAB IntersurgicalINTERSURGICAL UAB. · UAB INTERSURGICAL | 20 | 2009–2023 | Pure Global AI |
| Brazil | ANVISA | Manufacturer | UAB INTERSURGICAL | 4 | 2024–2026 | Pure Global AI |
| Tanzania | TMDA | Manufacturer | Intersurgical UAB | 1 | 2025–2025 | 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 Intersurgical UAB currently lists, by FDA device type, with the brand and model names on the listing.
| Device type | Category | Role | Brands and models | Listed since |
|---|---|---|---|---|
| Manual ToothbrushEFW · Class 1 | Toothbrushes | Maker | — | 2012 |
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 |
|---|---|---|
| UAB INTERSURGICALFDA reg. 3001313714 | PABRADE Svencionys, Lithuania | Contract manufacturer |
Other names on FDA records
UAB Intersurgical
Sources
FDA establishment registration & device listing (search FDA, owner/operator 9058058). 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.