FDA applicant

Rudolph Beaver, Inc.

Waltham, MA6 decisions1985–19880 recalls

FDA records 6 decisions for Rudolph Beaver, Inc. (Waltham, MA) from 1985 to 1988: 6 510(k) clearances. Most are in product codes HNN (Knife, Ophthalmic) and HRX (Arthroscope). 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 Rudolph Beaver, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Rudolph Beaver, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Rudolph Beaver, Inc.

Which product codes does it file in?

What has FDA decided for it lately?