510(k) Report

FDA applicant

J. T. Posey Co.

Arcadia, CA13 decisions1992–201224 recalls

FDA records 13 decisions for J. T. Posey Co. (Arcadia, CA) from 1992 to 2012: 13 510(k) clearances. Most are in product codes FMQ (Restraint, Protective) and OYS (Patient Bed With Canopy/Restraints). Its devices cite 5 predicates, 2 of them its own earlier devices. 24 recalls are 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 J. T. Posey Co.’s devices, and how often a recall has named them.

FDA decisions per year

2in 2012

2011: 12012: 2
2007high 2 (2012) · low 0 (2007)2026

2026 so far, outlined.

Recalls per year

22in 2009

2008: 22009: 22
2007high 22 (2009) · low 0 (2007)2026

Class I Class II/III not classified

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

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