510(k) Report

FDA applicant

Vine Valley Research

Middlesex, NY1 decision1989–19890 recalls

FDA records 1 decision for Vine Valley Research (Middlesex, NY) in 1989: 1 510(k) clearance. All are in product code EIL (Gauge, Depth, Instrument, Dental). 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, dental panel, where it files most

How often FDA has decided Vine Valley Research’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Vine Valley Research since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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