FDA applicant

Mercury Enterprises, Inc.

Clearwater, FL3 decisions1986–19890 recalls

FDA records 3 decisions for Mercury Enterprises, Inc. (Clearwater, FL) from 1986 to 1989: 3 510(k) clearances. Most are in product codes FMK (Single Use Only Blood Lancet With An Integral…) and FKY (Connector, Tubing, Dialysate). 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, gastroenterology and urology panel, where it files most

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

FDA decisions per year

No FDA decision for Mercury Enterprises, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Mercury Enterprises, 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 “Mercury”

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

Mercury Medical 16 Mercury Computer Systems, Inc. 2 Mercury Ent., Inc. D/B/A Mercury Medical 1 Mercury Enterprizes Dba Mercury Medical 1 Mercury Electronics (Scot), Ltd. 1

Mercury Enterprises, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Mercury”