DeviceClearance

Aribex, Inc.

Aribex, Inc. holds 3 FDA 510(k) medical device clearances, first cleared 2005, most recent 2014, with 2 FDA device recalls on record.

Top product codes for Aribex, Inc.

FDA recalls by Aribex, Inc.

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 Aribex, Inc.

Data sourced from openFDA. This site is unofficial and independent of the FDA.