FDA applicant

Webb Research Ii, Inc.

Philadelphia, PA2 decisions1993–20010 recalls

FDA records 2 decisions for Webb Research Ii, Inc. (Philadelphia, PA) from 1993 to 2001: 2 510(k) clearances. Most are in product codes GEI (Electrosurgical, Cutting & Coagulation &…) and KPR (System, X-Ray, Stationary). 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, general and plastic surgery panel, where it files most

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

FDA decisions per year

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

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Webb Research Ii, 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, Inc. 2

Webb Research Ii, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Webb”