KERR ITALIA SRL
IT-MF-000007768 · Italy · Scafati (SA)
KERR ITALIA SRL is registered in the European database on medical devices as a manufacturer, with 5 016 devices declared. It has a similarly named entry in the FDA register that we have not verified.
What this manufacturer declares
| Class IIa | 5 016 |
|---|
Among these devices, 679 are declared implantable, 3 622 reusable, 16 active.
Devices declared under this manufacturer
- Build-it FR
- Carbide Bur
- Diamond Bur
- Extruder Gun
- FibreKleer 4x Fiber Posts
- Flow It ALC
- Hand Files
- Herculite XRV Ultra
- K3 ENG FILE
- K3XF FILE
- Matrices and Wedges
- Paper Points
Showing 12 of 5 016 declared devices.
Catalogue references include 400113-JT0, 450108-BD5, 823-4450, FG7104-PLC, FGSS556-PL0, HP3-PLC.
European nomenclature codes declared: Q010399, Q01010103, Q010507, Q01010403, L159004, Q01010401.
United States market access
| FDA establishment register | Similar name found — unverified |
|---|---|
| Matched entry | Kerr Italia, S.r.l. (IT) · FDA 8020994 |
| Devices in EUDAMED | 5 016 |
| Country of registration | Italy |
⚠️ A similar name exists; we do not assert it is the same company — why.
Device-level evidence
| Devices with a numeric GTIN | 5 016 |
|---|---|
| Found in the U.S. device database | 9 |
| Share | 0.2 % |
Canadian market access
| Health Canada licence listing | Similar name found — unverified |
|---|---|
| Matched entry | KERR ITALIA S.R.L. |
⚠️ A similar name exists; unverified — why.
What it holds in Canada
| Licences on record | 15 |
|---|---|
| Currently active | 0 |
| Class 2 devices | 6 |
| Class 3 devices | 9 |
| First licensed | 1999-07-13 |
Licence types: Device Family (7), Device Group Family (4), System (3), Single Device (1).
Licensed under: SYSTEM B HEAT SOURCE, TEMPSPAN TEMPORARY CROWN AND BRIDGE MATERIAL, FLOW-IT ALC FLOWABLE COMPOSITE SYSTEM, BREEZE SELF-ADHESIVE CEMENT, SILANE, FIBREKLEER 4X FIBER POSTS.