| Symbol | GMED |
|---|---|
| Name | GLOBUS MEDICAL INC |
| Sector | HEALTH CARE |
| Region | North America |
| Industry | Surgical & Medical Instruments & Apparatus |
| Address | 2560 GENERAL ARMISTEAD AVENUE, AUDUBON, PA 19403 |
| Telephone | 610-930-1800 |
| Fax | — |
| — | |
| Website | https://www.globusmedical.com |
| Incorporation | UNDEFINED |
| Incorporated On | — |
| Employees | — |
| Fiscal Year | — |
| Public Since | — |
| Exchanges | NASDAQ |
| Auditor | — |
| Audit Status | NOT PROVIDED |
| Reporting Status | — |
| CIK | 0001237831 |
| Description | Globus Medical Inc is a medical device company that develops and provides healthcare products and solutions to hospitals, physicians, and surgical centers. The firms products are organized into two categories: musculoskeletal solutions, which include medical devices and instruments used mostly for spinal and orthopedic procedures, and enabling technologies, which include advanced computer systems developed for enhancing surgical capabilities. The vast majority of the companys revenue is generated from musculoskeletal solutions products, and more than half of the revenue is earned in the United States. Additional info from NASDAQ: |
New Form SCHEDULE 13G - GLOBUS MEDICAL INC <b>Filed:</b> 2026-04-30 <b>AccNo:</b> 0002100119-26-000630 <b>Size:</b> 7 KB
Read moreNew Form DEFA14A - GLOBUS MEDICAL INC <b>Filed:</b> 2026-04-24 <b>AccNo:</b> 0001628280-26-027200 <b>Size:</b> 359 KB
Read moreGlobus Medical Schedules First Quarter Earnings Release and Conference Call
Read more📋 DeFord John A (Ex-Director) plans to sell 30K shares of GLOBUS MEDICAL INC (at $93.10 each, total $2.8M) Filed: Apr 14, 2026 | ID: 000142
Read moreNew Form SCHEDULE 13G/A - GLOBUS MEDICAL INC <b>Filed:</b> 2026-03-26 <b>AccNo:</b> 0000102909-26-001392 <b>Size:</b> 7 KB
Read moreHuller Kelly 🟡 adjusted position in 20.0K shares (1 derivative) of GLOBUS MEDICAL INC (GMED) at $94.50 ($3.6M) Transaction Date: Feb 25, 2026 | Filing ID: 083348
Read more📋 Huller Kelly (Officer) plans to sell 20K shares of GLOBUS MEDICAL INC (at $94.45 each, total $1.9M) Filed: Feb 25, 2026 | ID: 000073
Read more| Trial ID | Title | Phase | Indication | Status | Start Date | Completion Date | Source |
|---|---|---|---|---|---|---|---|
| NCT06298812 | REFLECT Scoliosis System Post Approval Study | Na | Idiopathic Scoliosis | Recruiting | 2024-04-08 | 2032-03-31 | ClinicalTrials.gov |
| NCT04257279 | Prospective Robotic Global Research Study (PROGRESS) | Na | Lumbar Disc Disease | Unknown | 2019-12-18 | 2021-12-01 | ClinicalTrials.gov |
| NCT04088383 | Amnios™ RT Outcomes Study | Na | Plantar Fasciitis | Completed | 2019-09-10 | 2022-11-30 | ClinicalTrials.gov |
| NCT03230279 | Sacroiliac Joint Fusion Comparison Study | Na | Sacroiliac Joint Somatic Dysfunction | Withdrawn | 2018-09-01 | 2024-09-01 | ClinicalTrials.gov |
| NCT03371316 | Preliminary Investigation of ViaShield™ Amnion Patch as an Anti-Adhesive Barrie… | Na | Hemicraniectomies | Withdrawn | 2018-01-20 | 2018-01-30 | ClinicalTrials.gov |
| NCT03162666 | Patient Outcomes Using an Expandable Spacer | — | Degenerative Disc Disease | Withdrawn | 2017-02-28 | 2020-11-06 | ClinicalTrials.gov |
| NCT02184520 | A Prospective Randomized Postmarket Clinical Study of the TRANSITION Stabilizat… | Na | Acute Instabilities Thoracic, Lumbar and Sacral Spine | Terminated | 2016-04-19 | 2017-05-18 | ClinicalTrials.gov |
| NCT02388022 | A Retrospective Study Using CALIBER® TLIF Expandable Spacer in the Treatment of… | — | Degenerative Disc Disease | Completed | 2014-01-01 | 2016-03-01 | ClinicalTrials.gov |
| NCT01861899 | Treatment of Sacroiliac Dysfunction With SI-LOK® Sacroiliac Joint Fixation SI-S… | — | Joint Dysfunction | Completed | 2013-05-02 | 2019-04-11 | ClinicalTrials.gov |
| NCT02075554 | Study of an Expandable Interbody Device for the Lumbar Spine | Na | Degenerative Disc Disease | Completed | 2012-07-01 | 2017-02-01 | ClinicalTrials.gov |
| NCT02299323 | INDEPENDENCE Spacer for Lumbar Fusion | — | Degenerative Disc Disease | Completed | 2012-01-01 | 2016-08-01 | ClinicalTrials.gov |
| NCT01441999 | Proximal Junctional Kyphosis Following Long Instrumented Spinal Fusion: The Eff… | Na | Kyphosis | Withdrawn | 2011-10-01 | 2017-03-01 | ClinicalTrials.gov |
| NCT01198470 | TRIUMPH Lumbar Artificial Disc IDE: A Pilot Study | Na | Lumbar Degenerative Disc Disease | Completed | 2010-09-01 | 2016-12-01 | ClinicalTrials.gov |
| NCT01156675 | Study Evaluating the Safety and Effectiveness of the FLEXUS(TM) Interspinous Sp… | Na | Lumbar Spinal Stenosis | Terminated | 2008-06-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT00527553 | The Effect of Eggs and Egg Products on Macular Pigment | Na | Age-related Macular Degeneration | Completed | 2007-10-01 | 2008-02-01 | ClinicalTrials.gov |
| NCT00401518 | A Pivotal Study of a Facet Replacement System to Treat Spinal Stenosis | Na | Lumbar Spinal Stenosis | Completed | 2006-10-01 | 2017-10-01 | ClinicalTrials.gov |
| NCT00243165 | Lifemel Honey to Reduce Leucopenia During Chemotherapy | Phase2 | Breast Cancer | Unknown | 2005-11-01 | — | ClinicalTrials.gov |
| NCT00882661 | SECURE®-C Cervical Artificial Disc Clinical Study/ SECURE-C Cervical Artificial… | Na | Symptomatic Cervical Disc Disease | Completed | 2005-07-01 | 2017-02-01 | ClinicalTrials.gov |
| Product Name | Type | Development Stage | Therapeutic Area | Study Status | Trial ID |
|---|---|---|---|---|---|
| REVERE | Other | Approved | Acute Instabilities Thoracic, Lumbar and Sacral Spine | TERMINATED | NCT02184520 |
| TRANSITION | Other | Approved | Acute Instabilities Thoracic, Lumbar and Sacral Spine | TERMINATED | NCT02184520 |
| Lifemel honey intake every day | Other | Phase PHASE2 | Breast Cancer | UNKNOWN | NCT00243165 |
| Lifemel honey intake every day | Other | Phase PHASE2 | Breast Cancer | UNKNOWN | NCT00243165 |
| Degenerative Disc Disease | Other | Preclinical | Degenerative Disc Disease | COMPLETED | NCT02388022 |
| INDEPENDENCE | Other | Preclinical | Degenerative Disc Disease | COMPLETED | NCT02299323 |
| ViaShield | Other | Approved | Hemicraniectomies | WITHDRAWN | NCT03371316 |
| egg product from enriched eggs | Other | Approved | Age-related Macular Degeneration | COMPLETED | NCT00527553 |
| zeaxanthin | Other | Approved | Age-related Macular Degeneration | COMPLETED | NCT00527553 |
| lutein | Other | Approved | Age-related Macular Degeneration | COMPLETED | NCT00527553 |
| not enriched egg | Other | Approved | Age-related Macular Degeneration | COMPLETED | NCT00527553 |
| egg product from enriched eggs | Other | Approved | Age-related Macular Degeneration | COMPLETED | NCT00527553 |
| zeaxanthin | Other | Approved | Age-related Macular Degeneration | COMPLETED | NCT00527553 |
| lutein | Other | Approved | Age-related Macular Degeneration | COMPLETED | NCT00527553 |
| not enriched egg | Other | Approved | Age-related Macular Degeneration | COMPLETED | NCT00527553 |
| XSTOP® Interspinous Spacer | Other | Approved | Lumbar Spinal Stenosis | TERMINATED | NCT01156675 |
| FLEXUS(TM) Interspinous Spacer | Other | Approved | Lumbar Spinal Stenosis | TERMINATED | NCT01156675 |
| Sacroiliac joint radiofrequency ablation | Other | Approved | Sacroiliac Joint Somatic Dysfunction | WITHDRAWN | NCT03230279 |
| Sacroiliac joint fusion | Other | Approved | Sacroiliac Joint Somatic Dysfunction | WITHDRAWN | NCT03230279 |
| TRIUMPH® Lumbar Artificial Disc | Other | Approved | Lumbar Degenerative Disc Disease | COMPLETED | NCT01198470 |
| Rigid Rod | Other | Approved | Kyphosis | WITHDRAWN | NCT01441999 |
| Less rigid rod | Other | Approved | Kyphosis | WITHDRAWN | NCT01441999 |
| SI-LOK | Other | Preclinical | Joint Dysfunction | COMPLETED | NCT01861899 |
| CALIBER | Other | Approved | Degenerative Disc Disease | COMPLETED | NCT02075554 |
| ALTERA | Other | Preclinical | Degenerative Disc Disease | WITHDRAWN | NCT03162666 |
| ExcelsiusGPS™ | Other | Approved | Lumbar Disc Disease | UNKNOWN | NCT04257279 |
| Saline | Other | Approved | Plantar Fasciitis | COMPLETED | NCT04088383 |
| Amnios™ RT | Other | Approved | Plantar Fasciitis | COMPLETED | NCT04088383 |
| REFLECT Scoliosis Correction System | Other | Approved | Idiopathic Scoliosis | RECRUITING | NCT06298812 |
| REFLECT Scoliosis Correction System | DEVICE | Approved | Idiopathic Scoliosis | RECRUITING | NCT06298812 |
| ExcelsiusGPS™ | PROCEDURE | Approved | Lumbar Disc Disease | UNKNOWN | NCT04257279 |
| Index or spine revision surgery for complex adult spinal deformity | PROCEDURE | Preclinical | Adult Spinal Deformity | RECRUITING | NCT04194138 |
| Saline | OTHER | Approved | Plantar Fasciitis | COMPLETED | NCT04088383 |
| Amnios™ RT | OTHER | Approved | Plantar Fasciitis | COMPLETED | NCT04088383 |
| ViaShield | BIOLOGICAL | Approved | Hemicraniectomies | WITHDRAWN | NCT03371316 |
| Sacroiliac joint radiofrequency ablation | PROCEDURE | Approved | Sacroiliac Joint Somatic Dysfunction | WITHDRAWN | NCT03230279 |
| Sacroiliac joint fusion | PROCEDURE | Approved | Sacroiliac Joint Somatic Dysfunction | WITHDRAWN | NCT03230279 |
| ALTERA | DEVICE | Preclinical | Degenerative Disc Disease | WITHDRAWN | NCT03162666 |
| Degenerative Disc Disease | DEVICE | Preclinical | Degenerative Disc Disease | COMPLETED | NCT02388022 |
| INDEPENDENCE | DEVICE | Preclinical | Degenerative Disc Disease | COMPLETED | NCT02299323 |
| Rigid Rod | DEVICE | Approved | Kyphosis | WITHDRAWN | NCT01441999 |
| Less rigid rod | DEVICE | Approved | Kyphosis | WITHDRAWN | NCT01441999 |
| REVERE | DEVICE | Approved | Acute Instabilities Thoracic, Lumbar and Sacral Spine | TERMINATED | NCT02184520 |
| TRANSITION | DEVICE | Approved | Acute Instabilities Thoracic, Lumbar and Sacral Spine | TERMINATED | NCT02184520 |
| CALIBER | DEVICE | Approved | Degenerative Disc Disease | COMPLETED | NCT02075554 |
| SI-LOK | DEVICE | Preclinical | Joint Dysfunction | COMPLETED | NCT01861899 |
| TRIUMPH® Lumbar Artificial Disc | DEVICE | Approved | Lumbar Degenerative Disc Disease | COMPLETED | NCT01198470 |
| XSTOP® Interspinous Spacer | DEVICE | Approved | Lumbar Spinal Stenosis | TERMINATED | NCT01156675 |
| FLEXUS(TM) Interspinous Spacer | DEVICE | Approved | Lumbar Spinal Stenosis | TERMINATED | NCT01156675 |
| ASSURE Cervical plate and an allograft interbody spacer | DEVICE | Approved | Symptomatic Cervical Disc Disease | COMPLETED | NCT00882661 |
| SECURE-C Cervical Artificial Disc | DEVICE | Approved | Symptomatic Cervical Disc Disease | COMPLETED | NCT00882661 |
| Randomized Instrumented posterolateral fusion (PLF) | DEVICE | Approved | Lumbar Spinal Stenosis | COMPLETED | NCT00401518 |
| Randomized ACADIA® Facet Replacement System | DEVICE | Approved | Lumbar Spinal Stenosis | COMPLETED | NCT00401518 |
| Non-randomized ACADIA® Facet Replacement System | DEVICE | Approved | Lumbar Spinal Stenosis | COMPLETED | NCT00401518 |