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 13, 2026, FDA's public records list Glustitch, Inc. with 5 510(k) clearances. The most recent is a 510(k) clearance dated Jan 14, 2016: GluStitch Twist Tissue Adhesive.
| Date | Record | Source |
|---|---|---|
| Jan 14, 2016 | GluStitch Twist Tissue AdhesiveK150032 · MPN | 510(k) clearances |
| Feb 23, 2009 | GLUSEAL 90, MODEL GLU9010K083752 · KMF | 510(k) clearances |
| Oct 10, 2007 | PERIACRYL 90,80,70,60, MODEL9010, 8020, 7030, 6040K071484 · EMA | 510(k) clearances |
| Aug 21, 2003 | GLUSEAL 5ML DISPENSER, 1 ML DISPENSER, .2 ML DISPENSERK030574 · KMF | 510(k) clearances |
| Dec 20, 2001 | GLUSITE, MODEL GLU002K013446 · EMA | 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
