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Sign in to claim this brandTransamerican Technologies International
United States·US-MF-000007955
Last updated September 17, 2026
About
TTI Medical is a manufacturer of camera adapters for microscopes, CO₂ laser accessories, fiberoptic handpieces, and surgical instruments.
From the manufacturer's own website. Source
What Transamerican Technologies International makes
The company manufactures reusable surgical accessories for laser systems, including beam guides, adaptors, and handpieces for irrigation, aspiration, and electrosurgical applications. It also produces laparoscopic laser couplers, endoscopic bipolar electrodes, camera holders, and surgical camera lenses designed for use in minimally invasive and open surgical procedures.
The portfolio includes devices classified as Class I and Class II under FDA regulations, with all products listed in the FDA’s Unique Device Identifier (UDI) database. The manufacturer is based 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 Transamerican Technologies International manufacture?
Transamerican Technologies International specializes in reusable surgical accessories for laser systems. These include surgical camera holders, laser adaptors, beam guides, irrigation/aspiration handpieces, laparoscopic laser couplers, and endoscopic bipolar electrodes. The company also produces surgical camera lenses and beam-focus handpieces, primarily designed for use in minimally invasive and open surgical procedures.
Where is Transamerican Technologies International based?
The company is headquartered in the United States. This location allows it to comply with U.S. regulatory requirements, including the classification and listing of its devices in the FDA’s Unique Device Identifier (UDI) database.
Which regulatory registries list Transamerican Technologies International’s devices?
All of Transamerican Technologies International’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. This registry ensures traceability and transparency for healthcare providers and regulatory bodies, as required for Class I and Class II devices.
How are Transamerican Technologies International’s devices classified under FDA regulations?
The company’s devices fall into two main FDA classification categories: Class I and Class II. Class I devices generally pose minimal risk and require general controls, while Class II devices involve a higher level of risk and may require special controls to ensure safety and effectiveness. Classification depends on factors like the device’s intended use and potential health impact.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- United States
- Address
- 220, Porter Drive, San Ramon, United States
- Website
- www.ttimedical.com
- linkedin.com/company/tti-medical
- —
- [email protected]
- Phone
- +1 925 553 7828
- PRRC Contact
- Ross Howes
- EUDAMED SRN
- US-MF-000007955
- FDA FEI Number
- 2938071
- DUNS Number
- —
Catalogue (484)
Page 3 of 10| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Accu-Beam | 7040 | FDA UDI | Class II | Active |
| Accu-Beam | 096089 | FDA UDI | Class II | Active |
| Accu-Beam | 9440F025 | FDA UDI | Class II | Active |
| Accu-Beam | 1103 | FDA UDI | Class II | Active |
| Accu-Beam | 8186 | FDA UDI | Class I | Active |
| Accu-Beam | 31260-532L | FDA UDI | Class I | Active |
| Accu-Beam | 3113WOL8 | FDA UDI | Class II | Active |
| Accu-Beam | 8112 | FDA UDI | Class I | Active |
| Accu-Beam | 6108 | FDA UDI | Class II | Active |
| Accu-Beam | 6150 | FDA UDI | Class II | Active |
| Accu-Beam | 9302 | FDA UDI | Class II | Active |
| Accu-Beam | 3181AS5-002 | FDA UDI | Class II | Active |
| Accu-Beam | 8131 | FDA UDI | Class I | Active |
| Accu-Beam | 9303 | FDA UDI | Class II | Active |
| Accu-Beam | C-ADPTR | FDA UDI | Class I | Active |
| Accu-Beam | 1059790 | FDA UDI | Class II | Active |
| Accu-Beam | 205-023-3 | FDA UDI | Class II | Unknown |
| Accu-Beam | 8194101-02 | FDA UDI | Class I | Active |
| FiberLase | AC-1059640 | FDA UDI | Class II | Active |
| Accu-Beam | 9301 | FDA UDI | Class II | Active |
| Accu-Beam | 9354-01 | FDA UDI | Class II | Active |
| Accu-Beam | 9450L | FDA UDI | Class II | Active |
| Accu-Beam | 1059784 | FDA UDI | Class II | Active |
| Accu-Beam | 1059781 | FDA UDI | Class II | Active |
| Accu-Beam | 1108 | FDA UDI | Class II | Active |
| Accu-Beam | 8100-1 | FDA UDI | Class I | Active |
| Accu-Beam | 7054 | FDA UDI | Class II | Active |
| Accu-Beam | 1059721 | FDA UDI | Class II | Active |
| Accu-Beam | 360131 | FDA UDI | Class II | Active |
| Accu-Beam | 9307 | FDA UDI | Class II | Active |
| Accu-Beam | 95397 | FDA UDI | Class II | Active |
| Accu-Beam | 721-1437-002 | FDA UDI | Class I | Active |
| Accu-Beam | 7083 | FDA UDI | Class II | Active |
| Accu-Beam | 7080 | FDA UDI | Class II | Active |
| Accu-Beam | 096082 | FDA UDI | Class II | Active |
| Accu-Beam | 9351-01 | FDA UDI | Class II | Active |
| Accu-Beam | 1059800 | FDA UDI | Class II | Active |
| Accu-Beam | 3113STR5 | FDA UDI | Class II | Active |
| Accu-Beam | 3113CAB6 | FDA UDI | Class II | Active |
| Accu-Beam | 301513-9901R | FDA UDI | Class I | Active |
| Accu-Beam | 04342043D | FDA UDI | Class II | Active |
| Accu-Beam | 1122 | FDA UDI | Class II | Active |
| Accu-Beam | 1059803 | FDA UDI | Class II | Active |
| Accu-Beam | 28321V | FDA UDI | Class I | Active |
| Accu-Beam | 8105 | FDA UDI | Class I | Active |
| Accu-Beam | 3181 | FDA UDI | Class II | Active |
| Accu-Beam | 8194104 | FDA UDI | Class I | Active |
| Accu-Beam | 3181AS5.1 | FDA UDI | Class II | Active |
| Accu-Beam | 7055003 | FDA UDI | Class II | Active |
| Accu-Beam | 7082 | FDA UDI | Class II | Active |
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