BRM Extremities SRL
Civate (LC) Lombardy, IT
BRM EXTREMITIES SRL appears in FDA device records in Civate (LC) Lombardy, IT. FDA records list 4 510(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 4 510(k) clearances for BRM Extremities SRL between 2020 and 2023. The busiest year on record is 2022, with 2. The most recent is 2023, with 1.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 2020 | 1 |
| 2022 | 2 |
| 2023 | 1 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K220142 | BRM Digitalis Spacer | KYJ | Substantially Equivalent | |
| K222820 | BRM TOOL Screws, BIOPLAN Subtalar Implant | HWC | Substantially Equivalent | |
| K203773 | BRM TOOL Screws | HWC | Substantially Equivalent | |
| K191966 | NewPrim System | KWH | Substantially Equivalent |
Registered establishments
| Registration | FEI | Establishment | Address | Registration expires | Product codes listed |
|---|---|---|---|---|---|
| 3016669046 | 3016669046 | BRM EXTREMITIES SRL | Via Privata ai Campi, 7, Civate (LC) Lombardy 23862 IT | 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