Data / Medical devices / United States / Transamerican Technologies International
Transamerican Technologies International: FDA-registered device maker in San Ramon, CA, United States, 13 510(k) clearances
Transamerican Technologies International is registered with the FDA (registration 2938071) in San Ramon, CA, United States. It lists 12 device types. The FDA files 13 510(k) clearances under its listings, the newest dated August 20, 1997. Registered through 2027. FDA data exported November 2, 2026.
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- FDA registration number
- 2938071
- Address
- 220 Porter Drive Suite 120, San Ramon, CA, United States, 94583
- Owner or operator
- TTI MEDICAL (2938071)
- Roles
- Manufacturer, Repackager or relabeler
- First device listed
- December 3, 1992
- Registered through
- 2027
- Brand names listed
- ACCU-BEAM, ACCU-BEAM CO2 Laser Handpieces, ACCU-BEAM CO2 Laser Wave Guide, ACCU-BEAM Fiber Optic Handpiece, ACCU-BEAM Laparoscope Couplers, ACCU-BEAM Laser Fibers, ACCU-BEAM Micromanipulator, ACCU-Beam 300W Xenon Light Source and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Accessories, Photographic, For Endoscope (Exclude Light Sources) | FEM | 1 | Manufacturer | accessdata.fda.gov |
| Bronchoscope (Flexible Or Rigid) | EOQ | 2 | Repackager or relabeler | accessdata.fda.gov |
| Camera, Cine, Endoscopic, Without Audio | FWL | 1 | Repackager or relabeler | accessdata.fda.gov |
| Camera, Surgical And Accessories | KQM | 1 | Manufacturer | accessdata.fda.gov |
| Camera, Television, Microsurgical, Without Audio | FWD | 1 | Repackager or relabeler | accessdata.fda.gov |
| Electrosurgical, Cutting & Coagulation & Accessories | GEI | 2 | Manufacturer, Repackager or relabeler | accessdata.fda.gov |
| Lamps, Microscope | KEG | 1 | Repackager or relabeler | accessdata.fda.gov |
| Laparoscope, General & Plastic Surgery | GCJ | 2 | Manufacturer | accessdata.fda.gov |
| Laser, Surgical, Gynecologic | HHR | 2 | Manufacturer | accessdata.fda.gov |
| Light Source, Endoscope, Xenon Arc | GCT | 2 | Repackager or relabeler | accessdata.fda.gov |
| Powered Laser Surgical Instrument | GEX | 2 | Manufacturer, Repackager or relabeler | accessdata.fda.gov |
| Tray, Surgical, Instrument | FSM | 1 | Manufacturer | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| August 20, 1997 | K971677 | ACCU-SURG BI-POLAR ELECTRODES, L-HOOK, NEEDLE, BALL, BIPOLAR CORD | GEI | Substantially Equivalent | Transamerican Technologies Intl. | accessdata.fda.gov |
| November 13, 1996 | K963193 | ACCU-BEAM LASER BLOCK 301513BG385/BEAM SPLITTERS 301513BG39 | GEX | Substantially Equivalent | Transamerican Technologies Intl. | accessdata.fda.gov |
| May 31, 1995 | K952006 | ACCU-BEAM FIBER OPTIC HANDPIECE | GEX | Substantially Equivalent | Tti Medical | accessdata.fda.gov |
| May 24, 1995 | K951895 | ACCU-BEAM 300W XENON LIGHT SOURCE | GCT | Substantially Equivalent | Tti Medical | accessdata.fda.gov |
| February 24, 1995 | K945648 | ACCU-BEAM C02 LASER HANDPIECE | GEX | Substantially Equivalent | Tti Medical | accessdata.fda.gov |
| February 14, 1994 | K934398 | ACCU-BEAM TISSUE DRILL & ASPIRATION/INJECTION NEEDLE | GCJ | Substantially Equivalent | Transamerican Technologies Intl. | accessdata.fda.gov |
| June 1, 1993 | K921208 | ACCU-BEAM TUBE SET | GCJ | Substantially Equivalent | Tti Medical | accessdata.fda.gov |
| November 7, 1991 | K910978 | ACCU-BEAM LAPAROSCOPIC SYSTEM | GEI | Substantially Equivalent | Tti Medical | accessdata.fda.gov |
| February 22, 1990 | K895656 | ACCU-BEAM WAVEGUIDE | GEX | Substantially Equivalent | Tti Medical | accessdata.fda.gov |
| May 15, 1989 | K890922 | ACCU-BEAM YAG FIBER | GEX | Substantially Equivalent | Tti Medical | accessdata.fda.gov |
| March 9, 1987 | K870063 | CO2 LASER BRONCHOSCOPE SET | EOQ | Substantially Equivalent | Tti Medical | accessdata.fda.gov |
| March 5, 1987 | K870046 | DOUBLE PUNCTURE CO2 LASER LAPAROSCOPY SET | HHR | Substantially Equivalent | Tti Medical | accessdata.fda.gov |
| March 5, 1987 | K864378 | CO2 LASER MICROMANIPULATOR | HHR | Substantially Equivalent | Transamerican Technologies Intl. | accessdata.fda.gov |
Compare with other makers
- All makers of Powered Laser Surgical Instrument
- All makers of Laparoscope, General & Plastic Surgery
- All makers of Light Source, Endoscope, Xenon Arc
- All makers of Camera, Surgical And Accessories
- All makers of Bronchoscope (Flexible Or Rigid)
Updated August 20, 1997. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.