Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in United StatesLabelled 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 Bemis Manufacturing Co. with 12 510(k) clearances. The most recent is a 510(k) clearance dated Jul 11, 2002: NO-POKES NEEDLE SAFETY DEVICE.
| Jul 11, 2002 | NO-POKES NEEDLE SAFETY DEVICEK020921 · FMI | 510(k) clearances |
| Feb 14, 1997 | BEMIS TWO GALLON SHARPS CONTAINERK965248 · FMI | 510(k) clearances |
| Feb 11, 1997 | BEMIS TWO GALLON CHEMOTHERAPY CONTAINERK964858 · MMK | 510(k) clearances |
| Mar 28, 1996 | BEMIS ONE QUART PHLEBOTOMY CONTAINER (PART NUMBER 100)K960525 · MMK | 510(k) clearances |
| Nov 27, 1995 | SHARPS DISPOSAL CONTAINERSK953797 · MMK | 510(k) clearances |
| Jun 2, 1995 | IGHT AND ELEVEN GALLON SHARPS AND CHEMOTHERAPY CONTAINERSK950340 · MMK | 510(k) clearances |
| May 23, 1994 | SHARPS DISPOSAL CONTAINER/PHLEBOTOMYK941665 · MMK | 510(k) clearances |
| May 23, 1994 | SHARPS DISPOSABLE CONTAINERSK931664 · MMK | 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
