Ferndale Laboratories, Inc.

Ferndale Laboratories, Inc. holds 1 FDA 510(k) medical device clearance, cleared in 2007, with 1 FDA device recall on record.

Top product codes for Ferndale Laboratories, Inc.

FDA recalls by Ferndale Laboratories, 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 Ferndale Laboratories, Inc.

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