Medical device makerLabelled 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 15, 2026, FDA's public records list Medi-Plast International with 12 510(k) clearances. The most recent is a 510(k) clearance dated Feb 12, 1996: MEDI-PLAST 2 PORT MANIFOLD (RIGHT ON).
| Feb 12, 1996 | MEDI-PLAST 2 PORT MANIFOLD (RIGHT ON)K954284 · DTL | 510(k) clearances |
| Oct 23, 1987 | 10CC CONTROL SYRINGEK873588 · FMF | 510(k) clearances |
| Oct 22, 1986 | MEDI-PLAST DISPOSABLE MANIFOLDK863402 · DTL | 510(k) clearances |
| Jun 13, 1986 | FLUOROSCOPE BAND BAGK861785 · JAA | 510(k) clearances |
| Jun 11, 1985 | ARTERIAL-VENOUS COMPRESSION DRESSINGK851489 · | 510(k) clearances |
| Jul 6, 1984 | STERILE PAN SETK842136 · FRG | 510(k) clearances |
| Mar 15, 1984 | OPERATING ROOM TRAY SETK840021 · FSM | 510(k) clearances |
| Feb 4, 1984 | HEART CATHETERIZATION TRAY SETK840022 · DRE | 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
