Valmed SRL
Tovo di S.Agata Sondrio, IT
VALMED SRL appears in FDA device records in Tovo di S.Agata Sondrio, IT. FDA records list 8 510(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 8 510(k) clearances for Valmed SRL between 1993 and 2019. The busiest year on record is 2001, with 2. The most recent is 2019, with 1.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1993 | 1 |
| 2001 | 2 |
| 2002 | 1 |
| 2004 | 1 |
| 2011 | 1 |
| 2012 | 1 |
| 2019 | 1 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K181393 | Empty Eva Bag, models FVM0134BP, FVM0135BP, FVM0136BP, FVM0137BP, FVM0138BP, FVM0139BP, FVM0140BP, FVM0141BP | KPE | Substantially Equivalent | |
| K112148 | POWERED MUSCLE STIMULATOR | IPF | Substantially Equivalent | |
| K101412 | EVA TPN BAG | KPE | Substantially Equivalent | |
| K031611 | P4-FITNESS | NGX | Substantially Equivalent | |
| K022175 | P4 PHYSIO | IPF | Substantially Equivalent | |
| K010754 | NURSE'S ASSISTANT O.R. CONTROL SYSTEM | GCJ | Substantially Equivalent | |
| K010716 | VAL LUX 600 SURGICAL LIGHT (PLUS AND RS), MODEL ML600/S: SINGLE LIGHT HEAD, ML600/SS: SINGLE LIGHT HEAD, ML600/1D): DOUB | FSY | Substantially Equivalent | |
| K925336 | VALU-PLUS PAD | KNN | Substantially Equivalent |
Registered establishments
| Registration | FEI | Establishment | Address | Registration expires | Product codes listed |
|---|---|---|---|---|---|
| 3009128476 | 3009128476 | VALMED SRL | Via dell Industria 3, Tovo di S.Agata Sondrio 23030 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
There is no verification record for this company. Most companies on this site have none: a record exists only where a company asked to be verified and MDM ran the checks, so the absence of one says nothing about the company.
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Data as of , FDA export datePage updated Source: openFDA, public domain