MedtechSourcebook

SMITH & NEPHEW INC.

Contract manufacturer ยท Oklahoma City, OK

FDA-registered (openFDA, export of Oct 21, 2026) ISO 13485: not verified

2013Product codes first listed, by year (tallest: 1)2026
FDA registration
1643264 (openFDA record; or search FDA's registration database)
FEI number
1643264
Registered for
FDA registration year 2026
Establishment types
Manufacturer; Contract manufacturer; Remanufacturer; Repackager or relabeler
Owner or operator
Smith & Nephew, Inc. (FDA owner/operator no. 1020279)
Registered address
ENDOSCOPY, 76 S. MERIDIAN AVE., Oklahoma City, OK 73107
Contract listings
7 device listings, 3 product codes, first listed Aug 9, 2013
Certification
Not verified. We have no certification data for this facility yet.

Devices listed as contract work

Each row is an FDA product code this facility lists under its contract establishment type, with the date of its earliest such listing.

Product codeDevice (FDA name)ClassCategoryRoleFirst listed
FQHLavage, JetClass IIGeneral hospitalContract manufacturingAug 9, 2013
KMIMonitor, Bed PatientClass IGeneral hospitalContract manufacturingJun 30, 2022
OMPNegative Pressure Wound Therapy Powered Suction PumpClass IIGeneral and plastic surgeryContract manufacturingMay 11, 2015