DeviceEstablishmentPulse / report

Depuy Orthopaedics, Inc. (manufacturer, Warsaw, IN): 12 new FDA device listings, incl. prosthesis, shoulder, semi-constrained, metal/polymer cemented

Depuy Orthopaedics, Inc. (Warsaw, Indiana): 12 new FDA device listings, incl. prosthesis, shoulder, semi-constrained, metal/polymer cemented. Its amount of 12 is top-decile (95th percentile of 2,570 records). Dated 89 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: 12 · 95th percentile of 2,570 DeviceEstablishmentPulse records · 12.0x the median

Free preview: all 14 published fields of this record are shown below. Locked: 72 related IN DeviceEstablishmentPulse records and the 5-column CSV export.

FieldValue
EstablishmentDepuy Orthopaedics, Inc.
Owner / operatorDePuy Synthes, Inc.
RoleManufacturer
Establishment typesDevelop Specifications But Do Not Manufacture At This Facility; Manufacture Medical Device
LocationWarsaw, IN, US
New listings12
DevicesProsthesis, Shoulder, Semi-Constrained, Metal/Polymer Cemented; Prosthesis, Shoulder, Semi-Constrained, Metal/Polymer, Uncemented; Prosthesis, Shoulder, Hemi-, Humeral, Metallic Uncemented; Prosthesis, Shoulder, Non-Constrained, Metal/Polymer Cemented; Shoulder Prosthesis, Reverse Configuration; Prosthesis, Knee, Patello/Femorotibial, Semi-Constrained, Uncemented, Porous, Coated, Polymer/Metal/Polymer; Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer; Orthopedic Stereotaxic Instrument; Bone Cement; Prosthesis, Hip, Hemi-, Femoral, Metal/Polymer, Cemented Or Uncemented
Product codesKWS, MBF, HSD, KWT, PHX, MBH, JWH, OLO, LOD, KWY, MBB, KWL
Device classesClass II
Medical specialtiesOrthopedic, Neurology
First new listing2026-06-15
Latest new listing2026-08-07
FDA registration number1818910
Registration expires2027-12-31
amount percentile95th of 2,570 (median 1, 12.0x 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: 2026-08-07
  • 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: Depuy Orthopaedics, Inc. and 73 Indiana peers

  • Indiana DeviceEstablishmentPulse records like this one: 73
  • Depuy Orthopaedics, Inc.'s amount: 95th percentile of 2,570 records
  • Timing: Low: older than 30 days
  • Estimated pipeline if you contact every Indiana peer: $14,600 (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 Depuy Orthopaedics, Inc. in Warsaw, Indiana?

Depuy Orthopaedics, Inc. (Warsaw, IN), a manufacturer, added 12 FDA device listings between 2026-06-15 and 2026-08-07.

How does Depuy Orthopaedics, Inc. compare to other Indiana DeviceEstablishmentPulse records?

This is a top-decile record: its amount of 12 is 12.0x the median of 1 across 2,570 records. It is 89 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.

Depuy Orthopaedics, Inc. vs. top 3 peers

OrganizationLocationAmountPercentileRecord date
Depuy Orthopaedics, Inc.Warsaw, IN1295th2026-08-07
Boston Scientific CorporationCoventry, RI1093rd2026-10-16
Surgentec LLCBoca Raton, FL1596th2026-10-16
Paragon 28Englewood, CO992nd2026-10-08

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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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