Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in IrelandLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under its name, each linked to the record.
As of Nov 13, 2026, FDA's public records list Proxy Biomedical Ltd. with 6 510(k) clearances. The most recent is a 510(k) clearance dated Apr 30, 2018: VitaMESH Macroporous PP Surgical Mesh.
Drug approvals, 510(k) clearances, recalls and letters, 2017 to 2026 to date
A hatched bar is a year that is not over, so its count covers only part of the year.
| Date | Record | Source |
|---|---|---|
| Apr 30, 2018 | VitaMESH Macroporous PP Surgical MeshK172636 · FTL | 510(k) clearances |
| May 13, 2011 | VITAMESH (TM) BLUE LIGHTWEIGHT MACROPOROUS PP SURGICAL MESHK111121 · FTL | 510(k) clearances |
| Mar 28, 2006 | VITAMESH MACROPOROUS PP SURGICAL MESHK060520 · FTL | 510(k) clearances |
| Aug 11, 2005 | MODIFICATION TO MOTIFMESH SOFT TISSUE PATCHK052100 · FTL | 510(k) clearances |
| Jun 17, 2005 | POLYFORM SYNTHETIC MESHK051245 · OTO | 510(k) clearances |
| May 20, 2005 | MOTIFMESH SOFT TISSUE PATCHK050678 · FTL | 510(k) clearances |
Spellings are joined only when they reduce to the same name, or a reviewed source names the same company. Sharing an FDA establishment number (FEI) is not enough: contract sites make products for many firms. Facts marked AI were labelled by a language model from the firm's FDA names; everything else comes from FDA or Wikidata. How this page is built
