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 14, 2026, FDA's public records list S. Jackson, Inc. with 16 510(k) clearances. The most recent is a 510(k) clearance dated Sep 15, 2008: SUPRAMESH EXTRA.
| Sep 15, 2008 | SUPRAMESH EXTRAK080216 · FTL | 510(k) clearances |
| Sep 25, 1997 | STERILE SUPRAFOIL SMOOTH NYLON FOIL SHEETSK973379 · FTM | 510(k) clearances |
| Dec 17, 1993 | SUPRAMID SUTUREK931613 · GAR | 510(k) clearances |
| Dec 17, 1993 | MOPYLEN SUTUREK931614 · GAW | 510(k) clearances |
| Dec 17, 1993 | NYLAMID SUTUREK931612 · GAR | 510(k) clearances |
| Oct 20, 1992 | MOPYLENK922630 · GAW | 510(k) clearances |
| Oct 2, 1991 | N80-838 SUPRAMID EXTRA SUTUREK912429 · GAR | 510(k) clearances |
| Oct 25, 1990 | SUPRAMID EXTRA SUTURESK904052 · GAR | 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
