FDA applicant

R.H. Burton Co.

Grove City, OH19 decisions1992–19930 recalls

FDA records 19 decisions for R.H. Burton Co. (Grove City, OH) from 1992 to 1993: 19 510(k) clearances. Most are in product codes HJO (Biomicroscope, Slit-Lamp, Ac-Powered) and HLM (Instrument, Measuring, Lens, Ac-Powered). 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, ophthalmic panel, where it files most

How often FDA has decided R.H. Burton Co.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for R.H. Burton Co. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like R.H. Burton Co.’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

R.H. Burton Co.

Which product codes does it file in?

What has FDA decided for it lately?