Contract manufacturerModo Inc. (Tualatin, OR)OregonRadiologyObstetrics and gynecologyGastroenterology and urologyGeneral and plastic surgeryClass IClass II
Modo Inc.
Contract manufacturer ยท Tualatin, OR
FDA-registered (openFDA, export of Oct 21, 2026) ISO 13485: not verified
- FDA registration
- 3013875526 (openFDA record; or search FDA's registration database)
- FEI number
- 3013875526
- Registered for
- FDA registration year 2026
- Establishment types
- Manufacturer; Contract manufacturer
- Owner or operator
- Modo Inc (FDA owner/operator no. 10042825)
- Registered address
- 18355 SW Teton Ave, Tualatin, OR 97062
- Contract listings
- 5 device listings, 5 product codes, first listed Mar 19, 2014
- 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 code | Device (FDA name) | Class | Category | Role | First listed |
|---|---|---|---|---|---|
| IZD | Probe, Uptake, Nuclear | Class I | Radiology | Contract manufacturing | Dec 17, 2014 |
| KNF | Coagulator-Cutter, Endoscopic, Unipolar (And Accessories) | Class II | Obstetrics and gynecology | Contract manufacturing | Nov 5, 2018 |
| KNW | Instrument, Biopsy | Class II | Gastroenterology and urology | Contract manufacturing | Mar 19, 2014 |
| NEU | Marker, Radiographic, Implantable | Class II | General and plastic surgery | Contract manufacturing | Aug 11, 2026 |
| NEY | System, Ablation, Microwave And Accessories | Class II | General and plastic surgery | Contract manufacturing | Mar 20, 2019 |