510(k) Report

FDA applicant

Sra Developments, Ltd.

Ashburton, Devon, GB5 decisions2003–20220 recalls

FDA records 5 decisions for Sra Developments, Ltd. (Ashburton, Devon, GB) from 2003 to 2022: 5 510(k) clearances. Most are in product codes LFL (Instrument, Ultrasonic Surgical) and JDX (Instrument, Surgical, Sonic And…). Its devices cite 9 predicates, 3 of them its own earlier devices. 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 Sra Developments, Ltd.’s devices, and how often a recall has named them.

FDA decisions per year

1in 2022

2007: 22015: 12022: 1
2007high 2 (2007) · low 0 (2008)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2007.

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

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