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 Post Medical with 6 510(k) clearances. The most recent is a 510(k) clearance dated Apr 21, 1999: DIABETIC NEEDLE DISPOSAL, MODEL # PMSM - 950.
| Apr 21, 1999 | DIABETIC NEEDLE DISPOSAL, MODEL # PMSM - 950K990371 · FMI | 510(k) clearances |
| Aug 15, 1997 | SYRINGE NEEDLE REMOVER (S.N.R.)K972536 · FMI | 510(k) clearances |
| May 9, 1994 | AUTOMATIC NEEDLE DISCONECT (A.N.D.)K925086 · FMI | 510(k) clearances |
| Apr 29, 1994 | SHARPS CONTAINMENT SYSTEMK925816 · FMI | 510(k) clearances |
| Apr 28, 1983 | MALE EXTERNAL CATHETERK830946 · KNX | 510(k) clearances |
| Apr 12, 1983 | SYRINGE/NEEDLE DISPOS-BOX-CUTTER/CRIMPERK830947 · | 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
