Home › Device types › KQW
Goniometer, Nonpowered
FDA product code KQW · Class 1 · Orthopedic
102
Registered devices
4
Adverse events
0
Recalls
13
510(k) clearances
Devices with this code
Ambler Surgical — AMBLER SURGICAL CORP.CanarE – Clinic Wearable Device — Canary Medical USA LLCmymobility® Platform — Zimmer Us, Inc.PYRENEES® Cervical Plate System — VB Spine LLCPYRENEES® Cervical Plate System — VB Spine LLCRegatta® Plate — Seaspine Orthopedics Corporationmymobility® Platform — Zimmer Us, Inc.AESCULAP — Aesculap AGLUMEX — GF HEALTH PRODUCTS, INC.PYRENEES® Cervical Plate System — VB Spine LLCLUMEX — GF HEALTH PRODUCTS, INC.Medline — MEDLINE INDUSTRIES, INC.PYRENEES® Cervical Plate System — VB Spine LLCmymobility® Platform — Zimmer Us, Inc.mymobility® Platform — Zimmer Us, Inc.Novo Surgical Inc. — NOVO SURGICAL, INC.Lafayette Extendable Goniometer — LAFAYETTE INSTRUMENT COMPANY, INC.mymobility® Platform — Zimmer Us, Inc.mymobility® Platform — Zimmer Us, Inc.Professional Hand Evaluation Kit — LAFAYETTE INSTRUMENT COMPANY, INC.DELTA XTEND — DEPUY (IRELAND)ADC® — AMERICAN DIAGNOSTIC CORPGONIOMETER PERSONAL — ALIMED, INC.mymobility® Platform — Zimmer Us, Inc.
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