Terumo Corporation
Terumo Corporation holds FDA 510(k) medical device clearances, first cleared 2012, most recent 2026.
Top product codes for Terumo Corporation
Recent clearances by Terumo Corporation
- K252295 — Ryurei
- K250700 — Pen Injector Needle 32.5
- K250751 — DualView Catheter
- K240818 — R2P Radifocus Glidewire Advantage
- K240859 — Glidewire GT-R
- K190427 — Immucise
- K181369 — Immucise Intradermal Injection System
- K173799 — NaviCross 0.018
- K170417 — Glidewire GT
- K130280 — CAPIOX FX HOLLOW FIBER OXYGENATOR W/ RESERVOIR
- K130493 — CAPIOX RX05 HOLLOW FIBER OXYGENATOR/RESERVOIR
- K122544 — TERUMO SURFLASH SAFETY I.V. CATHETER
- K113335 — HEARTRAIL III GUIDING CATHETER
Data sourced from openFDA. This site is unofficial and independent of the FDA.