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 KMI Kolster Methods with 6 510(k) clearances. The most recent is a 510(k) clearance dated Oct 23, 2006: KOLSTER METHODS, INC., FEATHERLIFT SILHOUETTE SUTURE.
| Oct 23, 2006 | KOLSTER METHODS, INC., FEATHERLIFT SILHOUETTE SUTUREK060414 · GAW | 510(k) clearances |
| Mar 4, 2005 | FEATHERLIFT EXTENDED APTOS THREADK043591 · GAW | 510(k) clearances |
| Nov 19, 2001 | STARS2000 POWER CANNULAK012236 · QPB | 510(k) clearances |
| Aug 9, 2001 | XUB EXTERNAL ULTRASOUNDK010702 · IMI | 510(k) clearances |
| Nov 16, 2000 | SSW-STERILE SOLUTION WARMERK002859 · LHC | 510(k) clearances |
| Oct 15, 1999 | IRRIGATION OR INFUSION PUMP K PUMPK991203 · FRN | 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
