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Holder, Head, Radiographic

FDA product code IWY · Class 1 · Radiology

202
Registered devices
17
Adverse events
1
Recalls
10
510(k) clearances

Devices with this code

pearltec — Pearl Technology AGSCANCOAT — DOMICO MED-DEVICE, LLCN/A — DOMICO MED-DEVICE, LLCBlessing Cathay — BLESSING CATHAY CORPORATIONNA — DOMICO MED-DEVICE, LLCNA — DOMICO MED-DEVICE, LLCBlessing Cathay — BLESSING CATHAY CORPORATIONBlessing Cathay — BLESSING CATHAY CORPORATIONNA — DOMICO MED-DEVICE, LLCTIDI — TIDI PRODUCTS, LLCNurofit™ Head Support — QfixHillrom™ — Baxter Medical Systems GmbH + Co. KGNurofit Premiere™ — QfixDeRoyal — DEROYAL INDUSTRIES, INC.NA — DOMICO MED-DEVICE, LLCN/A — DOMICO MED-DEVICE, LLCNEUROLOGICA — TIDI PRODUCTS, LLCGE Healthcare — TIDI PRODUCTS, LLCTrumpf Medical — Baxter Medical Systems GmbH + Co. KGSCANCOAT — DOMICO MED-DEVICE, LLCCrania Adult — Pearl Technology AGNA — DOMICO MED-DEVICE, LLCNA — DOMICO MED-DEVICE, LLCNA — DOMICO MED-DEVICE, LLC

Recent recalls

DateFirmReason
2007-06-05Brainlab AGTarget Alignment Error : A mechanical component/software incompatibility caused by a specific combination of the BrainLAB Target Positioner version 40700-3A for

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Sourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.