FDA applicant

Vista Labs

Centralia, WA2 decisions1997–19970 recalls

FDA records 2 decisions for Vista Labs (Centralia, WA) in 1997: 2 510(k) clearances. All are in product code ESD (Hearing Aid, Air-Conduction, Prescription). 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, ear, nose and throat panel, where it files most

How often FDA has decided Vista Labs’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Vista Labs since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Vista Labs 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 AI, Inc. 2 Vista Med 1 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 Labs

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Vista”