FDA applicant

Ferring Laboratories, Inc.

Mchenry, IL2 decisions1983–19890 recalls

FDA records 2 decisions for Ferring Laboratories, Inc. (Mchenry, IL) from 1983 to 1989: 2 510(k) clearances. All are in product code FRN (Pump, Infusion). No recall is linked to its devices.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, general hospital panel, where it files most

How often FDA has decided Ferring Laboratories, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Ferring Laboratories, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Ferring Laboratories, Inc. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Ferring Laboratories, Inc.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

See the 510(k) Report

Other applicant names beginning “Ferring”

FDA records each applicant name separately; these may or may not be the same firm.

Ferring Pharmaceuticals, Inc. 1

Ferring Laboratories, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Ferring”