FDA applicant

The Sanborn Co.

Santa Clara, CA2 decisions1990–19900 recalls

FDA records 2 decisions for The Sanborn Co. (Santa Clara, CA) in 1990: 2 510(k) clearances. Most are in product codes HLR (Keratoscope, Battery-Powered) and HJA (Photokeratoscope). 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 The Sanborn Co.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for The Sanborn Co. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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The Sanborn Co.

Which product codes does it file in?

What has FDA decided for it lately?