Voco GmbH
Bend, OR, US
Voco GmbH appears in FDA device records in Bend, OR. FDA records list 13 510(k) clearances between and , no PMA records and no registered establishments. As of , FDA records show no recalls for this company.
FDA records held for this company
- 510(k) clearances
- 13
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 13 510(k) clearances for Voco GmbH between 2002 and 2005. The busiest year on record is 2002, with 4. The most recent is 2005, with 3.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 2002 | 4 |
| 2003 | 3 |
| 2004 | 3 |
| 2005 | 3 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K051868 | GRANDIO FLOW | EBF | Substantially Equivalent | |
| K051867 | GRANDIO | EBF | Substantially Equivalent | |
| K051535 | MODIFICATION TO:REGISTRADO X-TRA | ELW | Substantially Equivalent | |
| K042670 | FUTURABOND NR | KLE | Substantially Equivalent | |
| K042669 | IONOFIL PLUS AC | EMA | Substantially Equivalent | |
| K040769 | STRUCTUR 2 SC | EBG | Substantially Equivalent | |
| K033117 | GRANDIO FLOW | EBF | Substantially Equivalent | |
| K033068 | IONOFIL COLOR AC | EMA | Substantially Equivalent | |
| K030844 | FINAL VARNISH LC | KLE | Substantially Equivalent | |
| K022797 | TWINKY STAR | EBF | Substantially Equivalent | |
| K022066 | REGISTRADO X-TRA | ELW | Substantially Equivalent | |
| K021842 | ADMIRA SEAL | EBC | Substantially Equivalent | |
| K021844 | ADMIRA PROTECT | EBC | Substantially Equivalent |
Registered establishments
No FDA establishment registrations recorded against this company.
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