Proxy Biomedical , Ltd.
Proxy Biomedical , Ltd. appears in FDA public data with 0 recalls, 6 510(k) clearances, 5 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on April 30, 2018.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 6
- Inspections
- 5
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K172636 | VitaMESH Macroporous PP Surgical Mesh | April 30, 2018 |
| K111121 | VITAMESH (TM) BLUE LIGHTWEIGHT MACROPOROUS PP SURGICAL MESH | May 13, 2011 |
| K060520 | VITAMESH MACROPOROUS PP SURGICAL MESH | March 28, 2006 |
| K052100 | MODIFICATION TO MOTIFMESH SOFT TISSUE PATCH | August 11, 2005 |
| K051245 | POLYFORM SYNTHETIC MESH | June 17, 2005 |
| K050678 | MOTIFMESH SOFT TISSUE PATCH | May 20, 2005 |