Medical Device Manufacturer · CA , Montreal

Orthosoft Inc. (d/b/a) Zimmer CAS - FDA 510(k) Cleared Devices

18 submissions · 18 cleared · Since 2017
18
Total
18
Cleared
0
Denied

Orthosoft Inc. (d/b/a) Zimmer CAS has 18 FDA 510(k) cleared orthopedic devices. Based in Montreal, CA.

Latest FDA clearance: Feb 2026. Active since 2017.

Browse the complete list of FDA 510(k) cleared orthopedic devices from this manufacturer. Filter by specialty or product code using the sidebar.

18 devices
1–12 of 18
Signature? ONE System
K260104 · QHE Shoulder Arthroplasty Implantation System · Orthopedic
Feb 2026 22d
Rosa? Knee System
K251314 · OLO Orthopedic Stereotaxic Instrument · Orthopedic
Nov 2025 199d
ROSA? Knee System
K242864 · OLO Orthopedic Stereotaxic Instrument · Orthopedic
Oct 2024 28d
ROSA? Shoulder System
K233199 · OLO Orthopedic Stereotaxic Instrument · Orthopedic
Feb 2024 146d
Signature? ONE System
K232425 · QHE Shoulder Arthroplasty Implantation System · Orthopedic
Dec 2023 123d
OptiVu? ROSA? MxR
K230567 · SBF Orthopedic Augmented Reality · Orthopedic
Jun 2023 104d
ROSA Hip System
K231162 · LLZ System, Image Processing, Radiological · Radiology
May 2023 29d
Rosa Knee System
K230180 · OLO Orthopedic Stereotaxic Instrument · Orthopedic
Feb 2023 30d
OptiVu ROSA MxR
K220733 · SBF Orthopedic Augmented Reality · Orthopedic
Jul 2022 137d
ROSA? Knee System
K213708 · OLO Orthopedic Stereotaxic Instrument · Orthopedic
Apr 2022 149d
Signature? ONE System
K212560 · QHE Shoulder Arthroplasty Implantation System · Orthopedic
Oct 2021 60d
Signature ONE System
K200615 · QHE Shoulder Arthroplasty Implantation System · Orthopedic
Jun 2020 88d
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