Globus Medical, Inc. (manufacturer, Audubon, PA): 16 new FDA device listings, incl. thoracolumbosacral pedicle screw system

Globus Medical, Inc. (Audubon, Pennsylvania): 16 new FDA device listings, incl. thoracolumbosacral pedicle screw system. Its amount of 16 is top-decile (96th percentile of 2,570 records). Dated 91 days ago, it serves as a historical benchmark. Score 85/100. As of 2026-10-28, from openFDA device registration and listing endpoint (U.S. Food and Drug Administration).

Data as of · Compiled by Zalwin from openFDA device registration and listing endpoint (U.S. Food and Drug Administration)

amount: 16 · 96th percentile of 2,570 DeviceEstablishmentPulse records · 16.0x the median

Free preview: all 14 published fields of this record are shown below. Locked: 43 related PA DeviceEstablishmentPulse records and the 5-column CSV export.

FieldValue
EstablishmentGlobus Medical, Inc.
RoleManufacturer
Establishment typesManufacture Medical Device
LocationAudubon, PA, US
New listings16
DevicesThoracolumbosacral Pedicle Screw System; Appliance, Fixation, Spinal Interlaminal; Growing Rod System; Pedicle Screw Spinal System, Adolescent Idiopathic Scoliosis; Rod, Fixation, Intramedullary And Accessories; Screw, Fixation, Bone; Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer; Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer + Additive/Metal/Polymer + Additive; Prosthesis, Knee, Patello/Femorotibial, Semi-Constrained, Uncemented, Porous, Coated, Polymer/Metal/Polymer; Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Uncemented
Product codesNKB, KWP, PGM, OSH, HSB, HWC, JWH, OIY, MBH, LWJ, KWY, OQI, LPH, JDI, OQH
Device classesClass II
Medical specialtiesOrthopedic
Brand namesSCRIPT; PRECICE; ACTIFY 3D; TRIVANCE
First new listing2026-05-11
Latest new listing2026-08-05
FDA registration number3004142400
Registration expires2026-12-31
amount percentile96th of 2,570 (median 1, 16.0x median)
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CSV columns: Establishment · Role · New listings · Devices · Latest listing · official source URL

  • Source agency: openFDA device registration and listing endpoint (U.S. Food and Drug Administration)
  • Record date: 2026-08-05
  • Data refreshed: 2026-10-28
  • Refunds on request within 14 days

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LIVE PUBLIC DATA Source: openFDA device registration and listing endpoint (U.S. Food and Drug Administration) · Last refreshed: Wed, 28 Oct 2026 20:51:27 GMT

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Peer benchmark and outreach value: Globus Medical, Inc. and 44 Pennsylvania peers

  • Pennsylvania DeviceEstablishmentPulse records like this one: 44
  • Globus Medical, Inc.'s amount: 96th percentile of 2,570 records
  • Timing: Low: older than 30 days
  • Estimated pipeline if you contact every Pennsylvania peer: $8,800 (peers × rate × deal size; an estimate from your assumptions, not a forecast)

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85 / 100 Score

  • Brings its own devices to market: buys manufacturing, sterilization and QMS help.
  • Class II or III devices: QMS and regulatory demands.
  • Several new listings at once.
  • U.S. establishment.

What is the DeviceEstablishmentPulse record for Globus Medical, Inc. in Audubon, Pennsylvania?

Globus Medical, Inc. (Audubon, PA), a manufacturer, added 16 FDA device listings between 2026-05-11 and 2026-08-05.

How does Globus Medical, Inc. compare to other Pennsylvania DeviceEstablishmentPulse records?

This is a top-decile record: its amount of 16 is 16.0x the median of 1 across 2,570 records. It is 91 days old; check the official source for later updates before acting. Its Score of 85/100 puts it among the stronger signals in this feed.

Globus Medical, Inc. vs. top 3 peers

OrganizationLocationAmountPercentileRecord date
Globus Medical, Inc.Audubon, PA1696th2026-08-05
Surgentec LLCBoca Raton, FL1596th2026-10-16
Ge Parallel Design, Inc.Phoenix, AZ1997th2026-10-07
Boston Scientific CorporationCoventry, RI1093rd2026-10-16

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From the openFDA device registration and listing data, refreshed weekly. A listing shows a device an establishment says it makes or handles for the U.S. market; it is not FDA clearance or approval. Contact persons and street addresses are not stored. Verify in the FDA Establishment Registration and Device Listing database.

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