MedtechSourcebook

Bioventus LLC

Contract manufacturer ยท Cordova, TN

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

2021Product codes first listed, by year (tallest: 3)2026
FDA registration
3027669735 (openFDA record; or search FDA's registration database)
FEI number
3027669735
Registered for
FDA registration year 2026
Establishment types
Complaint file establishment; Manufacturer; Contract manufacturer; Repackager or relabeler
Owner or operator
Bioventus LLC (FDA owner/operator no. 10040666)
Registered address
7101 Goodlett Farms Pkwy, Cordova, TN 38016
Contract listings
14 device listings, 7 product codes, first listed Jul 27, 2021
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
BXBExerciser, PoweredClass IPhysical medicineContract manufacturingMay 31, 2022
GEIElectrosurgical, Cutting & Coagulation & AccessoriesClass IIGeneral and plastic surgeryContract manufacturingAug 18, 2023
GZIStimulator, Neuromuscular, External FunctionalClass IINeurologyContract manufacturingJul 27, 2021
IKKSystem, Isokinetic Testing And EvaluationClass IIPhysical medicineContract manufacturingJun 15, 2022
IPFStimulator, Muscle, PoweredClass IIPhysical medicineContract manufacturingJul 27, 2021
LFLInstrument, Ultrasonic SurgicalUnclassifiedGeneral and plastic surgeryContract manufacturingAug 18, 2023
PTYComputerized Cognitive Assessment Aid, ExemptClass IINeurologyContract manufacturingJul 11, 2022