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 Sil-Med Corporation with 29 510(k) clearances. The most recent is a 510(k) clearance dated Oct 1, 1997: NAVIGATOR (STYLET) 2006.
| Oct 1, 1997 | NAVIGATOR (STYLET) 2006K972521 · GAH | 510(k) clearances |
| Jul 18, 1997 | ANTIMICROBIAL PERITONEAL DIALYSIS COIL CATHETER WITH SPI-ARGENT IIK961392 · FJS | 510(k) clearances |
| Aug 8, 1996 | ANTIMICROBIAL MEDIASTINAL SILICONE DRAINK961194 · GBW | 510(k) clearances |
| Jun 26, 1996 | SAPPHIRE LINE FLAT DRAIN/KIT WITH SPI-ARGENT II W/OR W/OUT TROCARK961295 · GBX | 510(k) clearances |
| Mar 11, 1996 | PENROSE DRAIN MODELS 6001 - 6007K960099 · GCY | 510(k) clearances |
| Jan 23, 1996 | GRIP-A-BOOTSK955463 · LXZ | 510(k) clearances |
| Jan 4, 1996 | MEDIASTINAL SILICONE DRAINSK942709 · GBW | 510(k) clearances |
| May 24, 1995 | SIL-SLIP (COATED/REGULAR(NON-COATED)THORACIC DRAINK926496 · GBX | 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
