Tri W-G, Inc.
United StatesFDA applicant, unverified FDA FEI 1717548
- Devices
- 35
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
What Tri W-G, Inc. makes
Tri W-G, Inc. manufactures fluoroscopic tables with tilt or power tilting capabilities, treatment tables and modifications, elevating traction tables, paraffin treatment tables, exam/treatment tables, powered exercise equipment, hi-lo tilt tables, and radiographic/fluoroscopic tables.
The company's devices are classified as Class I and Class II medical devices and are listed in the FDA 510(k) registry. Tri W-G, Inc. is based in the United States.
Catalogue
Search and filter all 35 devicesCompany details
- FDA FEI number
- 1717548
- Address
- 215 12th Ave NE, VALLEY CITY, ND, 58072
Frequently asked questions
How many devices does Tri W-G, Inc. have in the registry?
The registry currently lists 35 devices for Tri W-G, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Tri W-G, Inc.'s devices?
Among its 35 most recently registered devices, Tri W-G, Inc. has devices listed in FDA 510(k) (35 devices).
What risk classes do Tri W-G, Inc.'s devices fall under?
Among its 35 most recently registered devices, the classes recorded for Tri W-G, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Tri W-G, Inc. in the registry?
The most recently registered devices listed for Tri W-G, Inc. include FLUOROSCOPIC TABLE, TILT OR POWER TILTING MED. TAB, TREATMENT TABLE MODIFICATION, R1436, R1697, R1699, R1564, R1216, R1214, R854 & R1213 and AUTORANGE MODEL 205.