FDA applicant

Vancouver Implant Center

V7k 2x4, CA3 decisions1995–19960 recalls

FDA records 3 decisions for Vancouver Implant Center (V7k 2x4, CA) from 1995 to 1996: 3 510(k) clearances. All are in product code 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 Vancouver Implant Center’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Vancouver Implant Center since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Vancouver Implant Center’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

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Other applicant names beginning “Vancouver”

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

Vancouver Implant Resources, Inc. 6 Vancouver Biotech, Ltd. 2

Vancouver Implant Center

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Vancouver”