Contract manufacturerINTERSON CORP. (Pleasanton, CA)CaliforniaRadiologyOrthopedicClass IIUnclassified
INTERSON CORP.
Contract manufacturer ยท Pleasanton, CA
FDA-registered (openFDA, export of Oct 21, 2026) ISO 13485: not verified
- FDA registration
- 2939830 (openFDA record; or search FDA's registration database)
- FEI number
- 1000124215
- Registered for
- FDA registration year 2027
- Establishment types
- Manufacturer; Contract manufacturer
- Owner or operator
- Interson Corporation (FDA owner/operator no. 9000675)
- Registered address
- 7150 Koll Center Pkwy, Pleasanton, CA 94566
- Contract listings
- 2 device listings, 4 product codes, first listed May 4, 2017
- 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 |
|---|---|---|---|---|---|
| ITX | Transducer, Ultrasonic, Diagnostic | Class II | Radiology | Contract manufacturing | May 4, 2017 |
| IYN | System, Imaging, Pulsed Doppler, Ultrasonic | Class II | Radiology | Contract manufacturing | May 4, 2017 |
| IYO | System, Imaging, Pulsed Echo, Ultrasonic | Class II | Radiology | Contract manufacturing | May 4, 2017 |
| LXC | Monitor, Pressure, Intracompartmental | Unclassified | Orthopedic | Contract manufacturing | Jun 21, 2024 |