Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in AustraliaLabelled 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 ITL Corporation with 5 510(k) clearances. The most recent is a 510(k) clearance dated Jun 23, 2016: Quiver Laparoscopic Extendable.
| Date | Record | Source |
|---|---|---|
| Jun 23, 2016 | Quiver Laparoscopic ExtendableK153472 · HAM | 510(k) clearances |
| Jul 2, 2002 | SAMPLOK LUER KITK021941 · JKA | 510(k) clearances |
| Jun 19, 2002 | LEESPEC DISPOSABLE VAGINAL SPECULUMK021017 · HIB | 510(k) clearances |
| Apr 11, 2000 | SAMPLOKK000777 · JKA | 510(k) clearances |
| May 14, 1999 | PLATYPUS AV FISTULA NEEDLE PROTECTOR (AVFNP)K991404 · FMI | 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
