MedtechSourcebook

Modo, Inc.

Contract manufacturer ยท McMinnville, OR

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

2016Product codes first listed, by year (tallest: 3)2026
FDA registration
3013875599 (openFDA record; or search FDA's registration database)
FEI number
3013875599
Registered for
FDA registration year 2026
Establishment types
Manufacturer; Contract manufacturer
Owner or operator
Modo Inc (FDA owner/operator no. 10042825)
Registered address
3280 NE Rivergate, McMinnville, OR 97128
Contract listings
4 device listings, 6 product codes, first listed Nov 7, 2016
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
BZNCart, Emergency, Cardiopulmonary (Excluding Equipment)Class IAnesthesiologyContract manufacturingSep 14, 2020
FOXStand, InfusionClass IGeneral hospitalContract manufacturingNov 7, 2016
GEIElectrosurgical, Cutting & Coagulation & AccessoriesClass IIGeneral and plastic surgeryContract manufacturingMar 13, 2018
HGIElectrocautery, Gynecologic (And Accessories)Class IIObstetrics and gynecologyContract manufacturingMar 13, 2018
HQCUnit, PhacofragmentationClass IIOphthalmicContract manufacturingAug 28, 2025
LFLInstrument, Ultrasonic SurgicalUnclassifiedGeneral and plastic surgeryContract manufacturingMar 13, 2018

Other contract facilities of Modo Inc