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 15, 2026, FDA's public records list Innovative Medical Technologies with 6 510(k) clearances. The most recent is a 510(k) clearance dated Sep 29, 2023: UltraFlo-R Push Button Blood Collection Set.
Drug approvals, 510(k) clearances, recalls and letters, 2017 to 2026 to date
A hatched bar is a year that is not over, so its count covers only part of the year.
| Sep 29, 2023 | UltraFlo-R Push Button Blood Collection SetK220458 · JKA | 510(k) clearances |
| Aug 27, 2013 | IMPROVE BLOOD COLLECTION SET AND IMPROSAFE BLOOD COLLECTION SETK123987 · JKA | 510(k) clearances |
| Sep 22, 1997 | QUICK-DRAW CAPILLARY WHOLE BLOOD COLLECTION SYSTEMK972969 · GIO | 510(k) clearances |
| Oct 20, 1994 | CARPAL BOXK936087 · KPR | 510(k) clearances |
| May 9, 1991 | RAPID IMMOBILIZATION DEVICE OR R.I.D. SYSTEMK904237 · FPP | 510(k) clearances |
| May 2, 1986 | IMT ULTRASONIC STRIDE MONITORK854194 · | 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
