Vilex, Inc.
Pleasant Hills, PA, US
Vilex, Inc. appears in FDA device records in Pleasant Hills, PA. FDA records list 6 510(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
- 6
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 6 510(k) clearances for Vilex, Inc. between 2002 and 2007. The busiest year on record is 2004, with 3. The most recent is 2007, with 1.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 2002 | 1 |
| 2004 | 3 |
| 2005 | 1 |
| 2007 | 1 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K070052 | MET-HEAD MODEL# MHDD-XX:CC DIAMETER, CC CANNULATION | KWD | Substantially Equivalent | |
| K052196 | VILEX X-FIX | KTT | Substantially Equivalent | |
| K041289 | TALUS OF VILEX (TOV) | HWC | Substantially Equivalent | |
| K041287 | VILEX BONE PLATE SYSTEM | HWC | Substantially Equivalent | |
| K023684 | CANNULATED METALLIC HEMI TOE IMPLANT, MODELS MPJ241975, MPJ221775, MPJ211675, MPJ191565, MPJ171365 | KWD | Substantially Equivalent | |
| K014154 | VILEX/DUVAL/ORTHEX CANNULATED BONE SCREW DB1 THREAD, MODEL F25-XX-09; VILEX SOLID BONE SCREWS DB1 THREAD,MODEL F20-XX-00 | HWC | 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