FDA applicant

Wells Johnson Co.

Tucson, AZ15 decisions1983–19990 recalls

FDA records 15 decisions for Wells Johnson Co. (Tucson, AZ) from 1983 to 1999: 15 510(k) clearances. Most are in product codes GEA (Cannula, Surgical, General & Plastic Surgery) and LFL (Instrument, Ultrasonic Surgical). 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 Wells Johnson Co.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Wells Johnson Co. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Wells”

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

Wells Lamont Corp. 4

Wells Johnson Co.

Which product codes does it file in?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “Wells”