U.S. Table, Inc.
United StatesFDA 510(k) applicant, unverified
- Devices
- 5
What U.S. Table, Inc. makes
U.S. Table, Inc. manufactures medical tables for patient positioning and therapy, including adjustable elevation therapy tables (e.g., PTT 6200) and specialized treatment tables (e.g., FLEX D-4000). Their portfolio also includes diagnostic and procedural tables, such as the ASH-7000 and EVT-3300 series, designed for imaging and therapeutic interventions. These devices support patient mobility, treatment positioning, and procedural stability in clinical settings.
The company’s products are regulated under the U.S. FDA’s 510(k) pathway, with devices classified as Class I and Class II. Their tables are listed in the FDA’s 510(k) database, adhering to U.S. medical device regulations. The manufacturer operates from the United States.
Catalogue
Ash-7000 Ref K951228
510(k) 510(k)Evt-3300 Ref K953621
510(k) 510(k)Ptt 6200 Elevation Therapy Table Ref K953622
510(k) 510(k)Flex D-4000 Ref K951419
510(k) 510(k)Evt-5000BX Ref K952600
510(k) 510(k)
Frequently asked questions
How many devices does U.S. Table, Inc. have in the registry?
The registry currently lists 5 devices for U.S. Table, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list U.S. Table, Inc.'s devices?
Among its 5 most recently registered devices, U.S. Table, Inc. has devices listed in FDA 510(k) (5 devices).
What risk classes do U.S. Table, Inc.'s devices fall under?
Among its 5 most recently registered devices, the classes recorded for U.S. Table, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from U.S. Table, Inc. in the registry?
The most recently registered devices listed for U.S. Table, Inc. include ASH-7000, EVT-3300, PTT 6200 ELEVATION THERAPY TABLE and FLEX D-4000.