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 13, 2026, FDA's public records list Megaplast, Inc. with 7 510(k) clearances. The most recent is a 510(k) clearance dated Oct 13, 1982: OPEN HEART TRAY (CUSTOM DESIGNED).
| Date | Record | Source |
|---|---|---|
| Oct 13, 1982 | OPEN HEART TRAY (CUSTOM DESIGNED)K822158 · KDD | 510(k) clearances |
| Jun 21, 1982 | SURGICAL UTILITY DRAPEK821313 · FJZ | 510(k) clearances |
| Mar 10, 1982 | SUTURE REMOVAL TRAYK820423 · KDD | 510(k) clearances |
| Jan 29, 1982 | URINARY DRAINAGE BAGK820136 · KNX | 510(k) clearances |
| Apr 7, 1981 | TRAY, CATHERIZATION, URETHRALK810249 · KOD | 510(k) clearances |
| Apr 7, 1981 | TRAY, IRRIGATIONK810250 · KNT | 510(k) clearances |
| Mar 11, 1981 | SYRINGE, ENTK810251 · KYZ | 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
