Origio A/S
Origio A/S holds FDA 510(k) medical device clearances, first cleared 2010, most recent 2020.
Top product codes for Origio A/S
Recent clearances by Origio A/S
- K200815 — VitriGuard
- K180740 — VitriGuard
- K173624 — ORIGIO® Handling without phenol red (Cat. No. 8310), ORIGIO® Handling with phenol red (Cat. No. 8311)
- K172197 — SAGE 1-Step GM-CSF with HSA, SAGE 1-Step GM-CSF with SPS
- K161547 — Transem and EchoGen Embryo Transfer Catheters
- K162833 — VitriGuard
- K153267 — ORIGIO Gradient 100, ORIGIO Gradient 90, ORIGIO Gradient 40/80, ORIGIO Sperm Wash
- K152932 — BlastGen
- K140317 — EMBRYOGEN
- K133912 — ORIGIO SEQUENTIAL FERT, ORIGIO SEQUENTIAL FERT WITH PHENOL RED, ORIGIO SEQUENTIAL CLEAV, ORIGIO SEQUENTIAL CLEAV, ORIGIO
- K133387 — ORIGIO(R) SEQUENTIAL BLAST TM; ORIGIO(R) SEQUENTIAL BLAST TM WITH PHENOL RED
- K133707 — SAGE 1-STEP WITH HUMAN SERUM ALBUMIN, SAGE 1-STEP WITH SERUM PROTEIN SUPPLEMENTS
- K120136 — EMBRYOGEN
- K100367 — MEDICULT VITRIFICATION COOLING/WARMING, MODEL REF: 1228, 1229
Data sourced from openFDA. This site is unofficial and independent of the FDA.