510(k) Report

FDA applicant

Advanced Diagnostics & Interventions

Redondo Beach, CA1 decision1999–19990 recalls

FDA records 1 decision for Advanced Diagnostics & Interventions (Redondo Beach, CA) in 1999: 1 510(k) clearance. All are in product code HRX (Arthroscope). 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, orthopedic panel, where it files most

How often FDA has decided Advanced Diagnostics & Interventions’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Advanced Diagnostics & Interventions since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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

See the 510(k) Report

Which product codes does it file in?

  • HRXArthroscope1decision

What has FDA decided for it lately?

  • K992621Adi 9000/9001 Arthroscope and AccessoriesAdvanced Diagnostics & Interventions · 1999

The one decision as Advanced Diagnostics & Interventions →