FDA applicant

Oxford Instruments, Plc.

Clearwater, FL7 decisions1994–20010 recalls

FDA records 7 decisions for Oxford Instruments, Plc. (Clearwater, FL) from 1994 to 2001: 7 510(k) clearances. Most are in product codes HEL (Monitor, Heart Rate, Fetal, Ultrasonic) and HGM (System, Monitoring, Perinatal). No recall is linked to its devices.

FDA’s records also spell it “Oxford Instruments”.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, obstetrics and gynecology panel, where it files most

How often FDA has decided Oxford Instruments, Plc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Oxford Instruments, Plc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Oxford”

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

Oxford Medilog, Inc. 48 Oxford Laboratories, Inc. 9 Oxford Performance Materials, Inc. 6 Oxford Instruments Medical Systems 5 Oxford Biosignals Limited 4 Oxford Metrics, Inc. 2 Oxford Medical, Inc. 2 Oxford Instruments Medical, Ltd. 1 Oxford Brain Diagnostics, Ltd. 1 Oxford Immunotec, Ltd. 1

Oxford Instruments, Plc.

Which product codes does it file in?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “Oxford”