OSMA's President discusses biocompatibility requirements, EU regulations, international market forces and audit preparations ahead of OMTEC 2024.

OSMA to Highlight Orthopedic Regulatory Issues at OMTEC

OSMA’s President discusses biocompatibility requirements, EU regulations, international market forces and audit preparations ahead of OMTEC 2024.

Stay up to date on the orthopedic market's 4Q performance in 2023 as we update this post with company sales data and industry developments.

Orthopedic Volume Trends Remained Strong in Fourth Quarter

Stay up to date on the orthopedic market’s 4Q performance in 2023 as we update this post with company sales data and industry developments.

While economic pressure slowed orthopedic funding in recent years, there is ample capital for enabling technology companies.

Orthopedic Funding Slows, Focuses on Digital

While economic pressure slowed orthopedic funding in recent years, there is ample capital for enabling technology companies.

Orthoflash®
The world's first TKA was performed using the STELLAR Knee mixed-reality surgical guidance system from PolarisAR.
First Total Knee with STELLAR Mixed-reality Surgical Guidance

The world’s first TKA was performed using the STELLAR Knee mixed-reality surgical guidance system from PolarisAR.

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Trivicta's triple-taper femoral stem supports an optimal fit within the canal for a diverse range of patient anatomies.
Ortho Development Gains FDA Clearance on Trivicta Hip

Trivicta’s triple-taper femoral stem supports an optimal fit within the canal for a diverse range of patient anatomies.

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BioPoly Radial Head
BioPoly Radial Head Receives FDA Clearance

This implant is manufactured from BioPoly’s proprietary material and is reported to be the only synthetic cartilage Radial Head on the market.

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RemeOs Spinal Interbody Cages are intended to restore intervertebral height and facilitate intervertebral body fusion in the cervical spine.
Bioretec RemeOs Granted Breakthrough Device Designation

RemeOs Spinal Interbody Cages are intended to restore intervertebral height and facilitate intervertebral body fusion in the cervical spine.

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BONESUPPORT CERAMENT G Synthetic Bone Graft Substitute
CERAMENT G Gains FDA 510(k) for Open Fracture Treatment

BONESUPPORT’s CERAMENT G synthetic bone graft substitute received FDA marketing clearance for use in open fractures.

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