Is this your brand? Sign in to claim ownership.
Sign in to claim this brandANALOGIC CORPORATION
US
Last updated May 27, 2026
What ANALOGIC CORPORATION makes
Analogic Corporation manufactures single-use probes for stereotactic surgery systems, including tracked and non-tracked variants designed for precision-guided procedures. The company also produces handheld ultrasound imaging systems for body-surface applications, such as the Sonic Window, along with sterile transducer covers for infection control. Additionally, it develops full-body computed tomography (CT) systems for detailed medical imaging.
The company’s devices are classified under FDA Class II regulations and are listed in the FDA’s 510(k) and Unique Device Identifier (UDI) databases. These products are intended for use in the United States, where the manufacturer is based.
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 Analogic Corporation manufacture?
Analogic Corporation specializes in three primary categories of medical devices: single-use stereotactic surgery system probes (including tracked and non-tracked variants), handheld ultrasound imaging systems for body-surface applications like the Sonic Window, and sterile transducer covers for ultrasound transducers. Additionally, the company develops full-body computed tomography (CT) systems for advanced imaging.
Where is Analogic Corporation based, and where are its devices primarily intended for use?
Analogic Corporation is based in the United States. The company’s devices are designed and intended for use within the U.S. regulatory environment, where they are subject to FDA oversight.
Which regulatory databases list Analogic Corporation’s devices?
Analogic Corporation’s devices are listed in the FDA’s 510(k) premarket notification database and the Unique Device Identifier (UDI) system. These registries help track and categorize medical devices that have undergone the necessary regulatory pathways for commercialization in the U.S.
How are Analogic Corporation’s devices classified under FDA regulations?
Analogic Corporation’s devices fall under FDA Class II classification. This classification typically applies to devices that pose moderate risk and require special controls beyond general controls to ensure their safety and effectiveness, such as performance standards or post-market surveillance.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
- Address
- —
- Website
- bkultrasound.com
- —
- —
- [email protected]
- Phone
- 1-604-279-8550
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- —
- DUNS Number
- 019677418
Catalogue (83)
Page 1 of 2| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Ultrasonix Medical Corporation | 00.035.064 | FDA UDI | Class II | Unknown |
| Ultrasonix Medical Corporation | 00.035.049 | FDA UDI | Class II | Unknown |
| Ultrasonix Medical Corporation | 20.000.000 | FDA UDI | Class II | Unknown |
| Pathfinder Shadow BK-T | 10-77322S-01 | FDA UDI | Class II | Active |
| Ultrasonix Medical Corporation | 18.000.000-02 | FDA UDI | Class II | Unknown |
| Ultrasonix Medical Corporation | 00.035.084 | FDA UDI | Class II | Unknown |
| Pathfinder Tracer | 10-77243S-01 | FDA UDI | Class II | Active |
| Ultrasonix Medical Corporation | 00.035.077 | FDA UDI | Class II | Unknown |
| Ultrasonix Medical Corporation | 00.035.056 | FDA UDI | Class II | Unknown |
| Ultrasonix Medical Corporation | 00.035.071 | FDA UDI | Class II | Unknown |
| Ultrasonix Medical Corporation | 21.000.000-02 | FDA UDI | Class II | Unknown |
| Ultrasonix Medical Corporation | 22.000.000 | FDA UDI | Class II | Unknown |
| Pathfinder Long Probe | 10-77242S-01 | FDA UDI | Class II | Active |
| Pathfinder Shadow (Aloka) | 10-77246S-01 | FDA UDI | Class II | Active |
| Pathfinder Beacon | 10-77248S-01 | FDA UDI | Class II | Active |
| Ultrasonix Medical Corporation | 00.035.077 | FDA UDI | Class II | Unknown |
| Sonic Window Handheld Ultrasound System | 10-73690-02 | FDA UDI | Class II | Active |
| Ultrasonix Medical Corporation | 21.000.000 | FDA UDI | Class II | Unknown |
| Sonic Window Sterile Transducer Cover | 21-05012-01 | FDA UDI | Class II | Active |
| Ultrasonix Medical Corporation | 00.035.058 | FDA UDI | Class II | Unknown |
| Ultrasonix Medical Corporation | 24.000.100 | FDA UDI | Class II | Unknown |
| Ultrasonix Medical Corporation | 00.035.069 | FDA UDI | Class II | Unknown |
| Ultrasonix Medical Corporation | 00.035.061 | FDA UDI | Class II | Unknown |
| Ultrasonix Medical Corporation | 00.035.072 | FDA UDI | Class II | Unknown |
| Ultrasonix Medical Corporation | 20.000.000-02 | FDA UDI | Class II | Unknown |
| Ultrasonix Medical Corporation | 00.035.073 | FDA UDI | Class II | Unknown |
| Pathfinder Tracked Probe | 10-77241S-01 | FDA UDI | Class II | Active |
| Analogic ImpaCT | 10-79182-01 | FDA UDI | Class II | Active |
| Ultrasonix Medical Corporation | 00.035.053 | FDA UDI | Class II | Unknown |
| Ultrasonix Medical Corporation | 24.000.000 | FDA UDI | Class II | Unknown |
| Pathfinder Shadow | 10-77247S-01 | FDA UDI | Class II | Active |
| Analogic ImpaCT | 10-78480-01 | FDA UDI | Class II | Active |
| Analogic ImpaCT | 10-79245-01 | FDA UDI | Class II | Active |
| Ultrasonix Medical Corporation | 00.035.063 | FDA UDI | Class II | Unknown |
| Sonic Window Docking Station | 10-73869-01 | FDA UDI | Class II | Active |
| Pathfinder Large Multi-Tool Instrument Clamp | 10-77249S-01 | FDA UDI | Class II | Active |
| Ultrasonix Medical Corporation | 00.024.634 | FDA UDI | Class II | Unknown |
| Sonic Window Handheld Ultrasound Unit | 10-73868-02 | FDA UDI | Class II | Active |
| Ultrasonix Medical Corporation | 00.035.066 | FDA UDI | Class II | Unknown |
| Pathfinder Small Multi-Tool Instrument Clamp | 10-77260S-01 | FDA UDI | Class II | Active |
| Ultrasonix Medical Corporation | 00.035.035 | FDA UDI | Class II | Unknown |
| Ultrasonix Medical Corporation | 18.000.000 | FDA UDI | Class II | Unknown |
| Ultrasonix Medical Corporation | 00.035.060 | FDA UDI | Class II | Unknown |
| Ultrasonix Medical Corporation | 22.000.000-02 | FDA UDI | Class II | Unknown |
| Anatom 2000 | K964890 | FDA 510(k) | Class II | Active |
| Patient Mon 1280/1281/120c/121c & Multi-Para Cart | K860646 | FDA 510(k) | Class II | Active |
| Synerad Impact 60, Synerad Impact 72 And Analogic Ams1600 | K052447 | FDA 510(k) | Class II | Active |
| C3 And Lifegard Icg Impedance Cardiography Monitors | K041434 | FDA 510(k) | Class II | Active |
| Dr9000 Digital Radiography X-Ray System | K001336 | FDA 510(k) | Class II | Active |
| System Sirecust 400 Siemens Sirecust 456-1a | K844791 | FDA 510(k) | Class II | Active |
Related Companies
Authorised Representatives
No authorised representatives on record.
Importers
Not available yet.
Notified Bodies
Not available yet.
Authorities
Not available yet.