Talladium Espana, SL
LLEIDA Lerida, ES
TALLADIUM ESPANA, SL appears in FDA device records in LLEIDA Lerida, ES. FDA records list 10 510(k) clearances between and , no PMA records and one registered establishment. As of , FDA records show no recalls for this company, and at least one establishment registration is current.
FDA records held for this company
510(k) clearance history
FDA records hold 10 510(k) clearances for Talladium Espana, SL between 2010 and 2026. The busiest year on record is 2023, with 2. The most recent is 2026, with 1.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 2010 | 1 |
| 2018 | 1 |
| 2021 | 1 |
| 2022 | 1 |
| 2023 | 2 |
| 2024 | 1 |
| 2025 | 2 |
| 2026 | 1 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K243732 | Multi-Unit DAS System | NHA | Substantially Equivalent | |
| K243425 | Guided DAS Surgical Kit | KCT | Substantially Equivalent | |
| K243530 | Dynamic TiBase | NHA | Substantially Equivalent | |
| K241170 | Dynamic TiBase; TRI Screws | NHA | Substantially Equivalent | |
| K231559 | Multi-Unit DAS System | NHA | Substantially Equivalent | |
| K232151 | Dynamic TiBase | NHA | Substantially Equivalent | |
| K221966 | Dynamic TiBase | NHA | Substantially Equivalent | |
| K212108 | Dynamic TiBase | NHA | Substantially Equivalent | |
| K162021 | 3.0 Dynamic TiBase | NHA | Substantially Equivalent | |
| K090081 | TALLADIUM INTERNATIONAL IMPLANTOLOGY ABUTMENTS | NHA | Substantially Equivalent |
Registered establishments
| Registration | FEI | Establishment | Address | Registration expires | Product codes listed |
|---|---|---|---|---|---|
| 3008517893 | 3008517893 | TALLADIUM ESPANA, SL | C/ Virginia Woolf 17, LLEIDA Lerida 25005 ES | 2026 |
Registration numbers link to the FDA registration and listing record for that establishment.
FDA product codes
Recall records
No recall records for this company in the ingested FDA data.
Verification record
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Data as of , FDA export datePage updated Source: openFDA, public domain