FDA applicant

Can-Am Surgical Corp.

Simi Valley, CA6 decisions1987–19870 recalls

FDA records 6 decisions for Can-Am Surgical Corp. (Simi Valley, CA) in 1987: 6 510(k) clearances. Most are in product codes FMF (Syringe, Piston) and FMI (Needle, Hypodermic, Single Lumen). 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 Can-Am Surgical Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Can-Am Surgical Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Can-Am Surgical Corp. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Can-Am Surgical Corp.’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

Can-Am Surgical Corp.

Which product codes does it file in?

What has FDA decided for it lately?