FDA applicant

Ind Ndiagnostic, Inc.

Delta, B.C., CA1 decision2012–20120 recalls

FDA records 1 decision for Ind Ndiagnostic, Inc. (Delta, B.C., CA) in 2012: 1 510(k) clearance. All are in product code NGT (Saline, Vascular Access Flush). 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, general hospital panel, where it files most

How often FDA has decided Ind Ndiagnostic, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

1in 2012

2012high 1 (2012) · low 0 (2013)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2012.

FIG. 1 — Ind Ndiagnostic, Inc. by year, 2012–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Ind Ndiagnostic, Inc.

Which product codes does it file in?

What has FDA decided for it lately?