FDA applicant

Hofa, LLC

Salt Lake City, UT1 decision1997–19970 recalls

FDA records 1 decision for Hofa, LLC (Salt Lake City, UT) in 1997: 1 510(k) clearance. All are in product code LCN (Scraper, Tongue). 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 Hofa, LLC’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Hofa, LLC since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Hofa, LLC’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

Hofa, LLC

Which product codes does it file in?

What has FDA decided for it lately?