DeviceEstablishmentPulse / report

Smith & Nephew Inc. (manufacturer, Oklahoma City, OK): 3 new FDA device listings, incl. intra-articular orthopedic stereotaxic navigation instrument

Smith & Nephew Inc. (Oklahoma City, Oklahoma): 3 new FDA device listings, incl. intra-articular orthopedic stereotaxic navigation instrument. Its amount of 3 is above the median of 1 (77th percentile). Dated 51 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: 3 · 77th percentile of 2,570 DeviceEstablishmentPulse records · 3.0x the median

Free preview: all 15 published fields of this record are shown below. Locked: 2 related OK DeviceEstablishmentPulse records and the 5-column CSV export.

FieldValue
EstablishmentSmith & Nephew Inc.
Owner / operatorSmith & Nephew, Inc.
RoleManufacturer
Establishment typesManufacture Medical Device
LocationOklahoma City, OK, US
New listings3
DevicesIntra-Articular Orthopedic Stereotaxic Navigation Instrument; Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer; Prosthesis, Knee, Patello/Femorotibial, Semi-Constrained, Uncemented, Porous, Coated, Polymer/Metal/Polymer
Product codesSIQ, JWH, MBH
Device classesClass II
Medical specialtiesOrthopedic
Brand names72205781 TESSA ACL Femur System License Software, No Cloud; 72205793 TESSA ACL Femur Straight Aimer Kit with ENDOBUTTON CL Ultra, 15mm; 72205778 TESSA ACL Femur Curved Aimer Kit; 72205801 TESSA ACL Femur Curved Aimer Kit with ULTRABUTTON QUAD Adjustable Fixation Device; 72205791 TESSA ACL Femur Straight Aimer Kit with ULTRABUTTON QUAD Adjustable Fixation Device; 72205777 TESSA ACL Femur Straight Aimer Kit; 72205782 TESSA Marker A; 72205455 INTELLIO Tablet
First new listing2026-07-30
Latest new listing2026-09-14
FDA registration number1643264
Registration expires2026-12-31
amount percentile77th of 2,570 (median 1, 3.0x 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: 2026-09-14
  • 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: Smith & Nephew Inc. and 3 Oklahoma peers

  • Oklahoma DeviceEstablishmentPulse records like this one: 3
  • Smith & Nephew Inc.'s amount: 77th percentile of 2,570 records
  • Timing: Low: older than 30 days
  • Estimated pipeline if you contact every Oklahoma peer: $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 Smith & Nephew Inc. in Oklahoma City, Oklahoma?

Smith & Nephew Inc. (Oklahoma City, OK), a manufacturer, added 3 FDA device listings between 2026-07-30 and 2026-09-14.

How does Smith & Nephew Inc. compare to other Oklahoma DeviceEstablishmentPulse records?

Its amount of 3 sits in the upper half (77th percentile) of 2,570 records; the median is 1. It is 51 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.

Smith & Nephew Inc. vs. top 3 peers

OrganizationLocationAmountPercentileRecord date
Smith & Nephew Inc.Oklahoma City, OK377th2026-09-14
Beacon Biosignals, Inc.Boston, MA377th2026-10-16
Endovascular Engineering, Inc.Menlo Park, CA377th2026-10-14
INNO Holdings Inc.Millcreek, UT377th2026-10-05

Related records

DeviceEstablishmentPulse: Manufacturer DeviceEstablishmentPulse: U.S. establishment DeviceEstablishmentPulse: records in Oklahoma

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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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