Vioptix, Inc.
Vioptix, Inc. holds FDA 510(k) medical device clearances, first cleared 2005, most recent 2025.
Top product codes for Vioptix, Inc.
Recent clearances by Vioptix, Inc.
- K250519 — Lap.Ox Laparoscopic Tissue Oximeter
- K233488 — Intra.Ox 2.0 Handheld Tissue Oximeter
- K221010 — Intra.Ox 2.0 Handheld Tissue Oximeter
- K191676 — Intra.Ox 2.0 Handheld Tissue Oximeter
- K163472 — Intra.Ox Handheld Tissue Oximeter
- K133983 — INTRA. OX HANDHELD TISSUE OXIMETER
- K141234 — ODISSEY TISSUE OXIMETER
- K090679 — VESSELINK MICROVASCULAR ANASTOMOTIC COUPLER SYSTEM
- K042657 — VIOPTIX ODISSEY TISSUE OXIMETER TISSUE OXIMETER, MODEL OXY-2
Data sourced from openFDA. This site is unofficial and independent of the FDA.