Data / Medical devices / United Kingdom / Topia Medtech Limited
Topia Medtech Limited: FDA-registered device maker in Welwyn Garden City Herefordshire, United Kingdom, 1 510(k) clearance
Topia Medtech Limited is registered with the FDA (registration 3043494619) in Welwyn Garden City Herefordshire, United Kingdom. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated December 19, 2025. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3043494619
- Address
- 2 Falcon Gate, Shire Park, Welwyn Garden City Herefordshire, United Kingdom, AL7 1TW
- Owner or operator
- Topia MedTech Limited (10094979)
- Roles
- Manufacturer
- First device listed
- January 12, 2026
- Registered through
- 2026
- Brand names listed
- Alzevita
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Automated Radiological Image Processing Software | QIH | 2 | Manufacturer | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| December 19, 2025 | K252670 | Alzevita | QIH | Substantially Equivalent | TOPIA MEDTECH LIMITED | accessdata.fda.gov |
Compare with other makers
Updated December 19, 2025. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.