510(k) Report

FDA applicant

Vident

Baldwin Park, CA36 decisions1990–20070 recalls

FDA records 36 decisions for Vident (Baldwin Park, CA) from 1990 to 2007: 36 510(k) clearances. Most are in product codes EIH (Powder, Porcelain) and DZE (Implant, Endosseous, Root-Form). 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 Vident’s devices, and how often a recall has named them.

FDA decisions per year

1in 2007

2007: 1
2007high 1 (2007) · low 0 (2008)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2007.

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

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