Gentian AS
Gentian AS holds FDA 510(k) medical device clearances, first cleared 2007, most recent 2008, with 1 FDA device recall on record.
Top product codes for Gentian AS
FDA recalls by Gentian AS
Recalls are matched by FDA's recalling-firm name — openFDA's enforcement dataset doesn't reference 510(k) numbers, so a recall here may cover devices beyond this company's 510(k) clearances.
Recent clearances by Gentian AS
Data sourced from openFDA. This site is unofficial and independent of the FDA.