510(k) Report

FDA applicant

Swiss American Metal Craft Corp.

Mchenry, IL4 decisions1980–19800 recalls

FDA records 4 decisions for Swiss American Metal Craft Corp. (Mchenry, IL) in 1980: 4 510(k) clearances. Most are in product codes EJL (Bur, Dental) and DZP (Instrument, Diamond, Dental). 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, dental panel, where it files most

How often FDA has decided Swiss American Metal Craft Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Swiss American Metal Craft Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Swiss American Metal Craft Corp. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Swiss American Metal Craft 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

Other applicant names beginning “Swiss”

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