FDA applicant

Webb Research, Inc.

Philadelphia, PA2 decisions1991–19950 recalls

FDA records 2 decisions for Webb Research, Inc. (Philadelphia, PA) from 1991 to 1995: 2 510(k) clearances. Most are in product codes KPR (System, X-Ray, Stationary) and LNH (System, Nuclear Magnetic Resonance Imaging). 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, radiology panel, where it files most

How often FDA has decided Webb Research, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Webb Research, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Webb”

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

Webb Research Ii, Inc. 2

Webb Research, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Webb”