Home › Device types › HXO
Pusher, Socket
FDA product code HXO · Class 1 · Orthopedic
154
Registered devices
58
Adverse events
1
Recalls
3
510(k) clearances
Devices with this code
NA — Zimmer, Inc.PINNACLE — DEPUY (IRELAND)SFS — Orthofix US LLCKHEIRON — S.M.A.I.OBIO-MODULAR CHOICE INSTRUMENTS — Biomet Orthopedics, LLCDSS™ Coupler Pusher — Paradigm Spine GmbHPINNACLE — DEPUY (IRELAND)Inion® Shoulder Instrumentation — Inion OyMEGA SPINE SYSTEM — BK MEDITECH CO.,LTD.PINNACLE — DEPUY (IRELAND)SPIROFIT PINNACLE — DEPUY (IRELAND)SPIROFIT PINNACLE — DEPUY (IRELAND)NexFix — TORNIER, INC.MEGA5.5 SPINE SYSTEM — BK MEDITECH CO.,LTD.ASCENT — Orthofix US LLCNatural Nail® — Zimmer, Inc.SPIROFIT PINNACLE — DEPUY (IRELAND)PINNACLE — DEPUY (IRELAND)SPIROFIT PINNACLE — DEPUY (IRELAND)SPIROFIT PINNACLE — DEPUY (IRELAND)LINER PUSHER HEAD — Biomet Uk LtdNA — Synthes GmbHHPS Rod pusher — Paradigm Spine GmbHTITAN™ — Ascension Orthopedics, Inc.
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2010-08-02 | Biomet, Inc. | The firm has received four complaints that the closed knot pusher is missing a radius which contributes to sutures being cut during surgery. |
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