Is this your brand? Sign in to claim ownership.
Sign in to claim this brandInterson Corporation
United States·US-MF-000020801
Last updated September 18, 2026
About
Interson develops and manufactures USB ultrasound probes for use in medical and veterinary settings that work on Windows-based devices. Manufactured in the USA.
From the manufacturer's own website. Source
What Interson Corporation makes
Interson Corporation manufactures hand-held extracorporeal ultrasound imaging transducers designed for rectal and vaginal use, as well as general-purpose ultrasound systems. Their portfolio includes software solutions such as SeeMore, SeeMore ViewBladder, Phantom Ultrasound Software, and I-Streme Echo, which integrate with Windows-based devices for medical and veterinary imaging applications.
The company’s devices are classified under EU Class II and Class IIa regulations, with listings in the EUDAMED database and the FDA’s Unique Device Identifier (UDI) system. Interson Corporation is headquartered in the United States.
Written from this company's registered devices by an AI model, and not verified by a human reviewer.
Frequently asked questions
What types of medical devices does Interson Corporation manufacture?
Interson Corporation specializes in extracorporeal ultrasound imaging devices. Their portfolio includes hand-held ultrasound transducers for rectal and vaginal use, as well as general-purpose ultrasound imaging systems. They also develop software solutions like SeeMore, SeeMore ViewBladder, Phantom Ultrasound Software, and I-Streme Echo, which are designed to integrate with Windows-based devices for medical and veterinary imaging. These devices are primarily focused on portable, USB-based ultrasound applications.
Where is Interson Corporation based?
Interson Corporation is headquartered in the United States. The company’s manufacturing and operations are conducted within the country, as indicated by its self-described focus on producing USB ultrasound probes ‘manufactured in the USA.’
Which regulatory registries list Interson Corporation’s devices?
Interson Corporation’s devices are listed in the EUDAMED database, which is the European Union’s medical device registry, and the FDA’s Unique Device Identifier (UDI) system in the United States. These registries help track and monitor medical devices for regulatory compliance and transparency.
How are Interson Corporation’s devices classified under medical device regulations?
Interson Corporation’s devices fall under EU Class II and Class IIa classifications. These classifications are determined by the risk associated with the device—Class IIa typically includes devices with a lower risk profile than Class II, though both require compliance with specific regulatory requirements to ensure safety and performance. The classification helps authorities and healthcare providers understand the oversight level required for these products.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- United States
- Address
- 7150 Koll Center Parkway, Pleasanton, United States
- Website
- www.interson.com
- linkedin.com/company/interson
- —
- [email protected]
- Phone
- +1 9254624948
- PRRC Contact
- Deepa Jethwaney
- EUDAMED SRN
- US-MF-000020801
- FDA FEI Number
- —
- DUNS Number
- —
Catalogue (36)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| SeeMore Software | 4.2.1 OB GYN | FDA UDI | Class II | Active |
| SeeMore | VC 7.5 MHz | FDA UDI | Class II | Active |
| SeeMore | GP 2000 | FDA UDI | Class II | Active |
| SeeMore Software 4.5. | x.x | FDA UDI | Class II | Active |
| SeeMore Software | 2.0.03 GEN | FDA UDI | Class II | Active |
| SeeMore | ER 12.0 MHz | FDA UDI | Class II | Active |
| Phantom Ultrasound Software | x.x | FDA UDI | Class II | Active |
| SeeMore Software | 2.0.03 OB GYN | FDA UDI | Class II | Active |
| I-Streme Echo Ultrasound Software | x.x | FDA UDI | Class II | Active |
| SeeMore Software | 4.2.1 URO | FDA UDI | Class II | Active |
| SeeMore ViewBladder 10 System | ViewBladder10 V2 | FDA UDI | Class II | Active |
| SeeMore | GP 5.0 MHz | FDA UDI | Class II | Active |
| VPS Rhythm DLX Ultrasound Probe | SP-DLX200 | FDA UDI | Class II | Active |
| I-Streme Echo Ultrasound System | 1 | FDA UDI | Class II | Active |
| SeeMore | PI 7.5 MHz | FDA UDI | Class II | Active |
| SeeMore ViewBladder 10 Software | 2.0.03 ViewBladder | FDA UDI | Class II | Active |
| SeeMore | ViewBladder 10 | FDA UDI | Class II | Active |
| SeeMore | EC 7.5 MHz | FDA UDI | Class II | Active |
| SeeMore | ES 12.0 MHz | FDA UDI | Class II | Active |
| SeeMore | MV 12 MHz | FDA UDI | Class II | Active |
| SeeMore Software | 4.2.1 GEN | FDA UDI | Class II | Active |
| SeeMore Software | 2.0.03 URO | FDA UDI | Class II | Active |
| SeeMore Software | 4.4.x | FDA UDI | Class II | Active |
| Interson Endocavity Probe/Kontron Ultrasound Syst | K911116 | FDA 510(k) | Class II | Active |
| Probe Sheath For Adms & Capistrano Labs Transrec. | K896680 | FDA 510(k) | Class II | Active |
| Biopsy Needle Guide For Adms Ultrasound Probes | K895725 | FDA 510(k) | Class II | Active |
| Interson Multiplane Rectal Probe For Aloka Ultra. | K900555 | FDA 510(k) | Class II | Active |
| Interson Transrectal Probe/Atl Ultrasound System | K911115 | FDA 510(k) | Class II | Active |
| Interson Endocavity Probe For Atl Ultrasound Syst | K911117 | FDA 510(k) | Class II | Active |
| Interson Disposable Biopsy Needle | K911464 | FDA 510(k) | Class II | Active |
| Interson Endocavity Probe/Aloka Ultrasound System | K911114 | FDA 510(k) | Class II | Active |
| Interson Transrectal Probe/Kontron Ultrasound Syst | K911113 | FDA 510(k) | Class II | Active |
| Interson USB Ultrasound Probe System | 99-9028-00 | EUDAMEDFDA UDI | Class IIa | Active |
| GP 3.5 MHz | 99-5929-00 | EUDAMEDFDA UDI | Class IIa | Active |
| Sp-L01 | 99-7901-00 | EUDAMEDFDA UDI | Class IIa | Active |
| Interson USB Ultrasound Probe System | 99-7903-00 | EUDAMEDFDA UDI | Class IIa | Active |
Related Companies
Authorised Representatives
Importers
Not available yet.
Notified Bodies
Not available yet.
Authorities
Not available yet.