FDA applicant

Vista Med

Charleston, SC1 decision1985–19850 recalls

FDA records 1 decision for Vista Med (Charleston, SC) in 1985: 1 510(k) clearance. All are in product code KNX (Collector, Urine, (And Accessories) For…). 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 Vista Med’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Vista Med since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Vista”

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

Vista Medical Technologies, Inc. 9 Vista Lifesciences, Inc. 2 Vista Labs 2 Vista AI, Inc. 2 Vista Laboratories, Inc. 1 Vista Ophthalmics, LLC 1 Vista Products, Inc. 1 Vista Scientific, LLC 1 Vista Vision 1 Vista Medical Products, Inc. 1 Vista Industries,, LLC 1

Vista Med

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Vista”