FDA Device Intelligence
Home › Device types › ISP

Valve, Prosthesis

FDA product code ISP · Class 1 · Physical Medicine

164
Registered devices
11
Adverse events
1
Recalls
1
510(k) clearances

Devices with this code

LimbLogic — Willowwood Global LLCLimbLogic — Willowwood Global LLCOne — Willowwood Global LLCLimbLogic — Willowwood Global LLCLimbLogic — Willowwood Global LLCOne — Willowwood Global LLCAria dummy plug insert — CYPRESS ADAPTIVE, LLCLimbLogic — Willowwood Global LLCAria Universal Mini Valve Key — CYPRESS ADAPTIVE, LLCLimbLogic — Willowwood Global LLCLimbLogic — Willowwood Global LLCAria Valve Plus (US) — CYPRESS ADAPTIVE, LLCAria plate valve gasket — CYPRESS ADAPTIVE, LLCAria Valve (US) — CYPRESS ADAPTIVE, LLCLimbLogic — Willowwood Global LLCAria Mini Valve — CYPRESS ADAPTIVE, LLCLimbLogic — Willowwood Global LLCLimbLogic — Willowwood Global LLCAria auto explusion valve insert kit — CYPRESS ADAPTIVE, LLCOne — Willowwood Global LLCAria Valve O-ring — CYPRESS ADAPTIVE, LLCLimbLogic — Willowwood Global LLCLimbLogic — Willowwood Global LLCOne — Willowwood Global LLC

Recent recalls

DateFirmReason
2009-06-23Ossur Engineering, IncThe plastic caps have come off or become loose when the user stepped into their prosthesis.

Query this across every FDA database — by API.

Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

Get your free API keyRead the docs
Sourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.