FDA applicant

Kinetix Instruments

Santa Clara, CA1 decision1994–19940 recalls

FDA records 1 decision for Kinetix Instruments (Santa Clara, CA) in 1994: 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 Kinetix Instruments’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Kinetix Instruments since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Kinetix Instruments’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

Other applicant names beginning “Kinetix”

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

Kinetix 4

Kinetix Instruments

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Kinetix”