KP Medical Ltd
UK-MF-000046954 · United Kingdom · MONMOUTH
KP Medical Ltd is registered in the European database on medical devices as a manufacturer, with 12 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 12 |
|---|
Most frequent device types declared: Dental Pod - White, Zima Go.
Among these devices, 5 are declared active.
Authorised representative in the Union: SMEDTEC OÜ.
Devices declared under this manufacturer
- Dental Pod
- Dental Pod Pro
- Invisalign Ultrasonic Cleaner
- Zima Dental Ultrasonic Boosting Tablets
- Zima Go UV Case
Catalogue references include DP-BLK-EU, DP-BLU-EU, DP-WHT-EU, DPP-BLK-EU, DPP-GRN-EU, DPP-WHT-EU.
European nomenclature codes declared: Z12011302, Z120614, V0799.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 12 |
| Country of registration | United Kingdom |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Device-level evidence
| Devices with a numeric GTIN | 12 |
|---|---|
| Found in the U.S. device database | 0 |
| Share | 0.0 % |
Canadian market access
| Health Canada licence listing | Not found in the Canadian register |
|---|
⚠️ Canada lists no Class I devices at all — what that excludes.
North American profile: Neither register. KP Medical Ltd was not found in either the U.S. or the Canadian register.