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Slenderizers Equipment Mfg., Inc.

United StatesFDA applicant, unverified

Devices
7

What Slenderizers Equipment Mfg., Inc. makes

Slenderizers Equipment Mfg., Inc. manufactures a series of adjustable, modular surgical tables under the Multi-Flex Table brand. These tables are designed for use in medical procedures requiring reconfiguration of patient positioning, including orthopedic, spinal, and general surgery applications. The models vary in features such as height adjustability, side rails, and integrated accessories for specialized positioning.

The company’s product portfolio is classified under FDA Class II devices and is listed via 510(k) clearance in the United States. The Multi-Flex Table models are registered with the FDA’s regulatory database, ensuring compliance with U.S. medical device regulations. The manufacturer operates from the United States.

AI-generated from registry data, 3 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue7

Newest first, rows 1-7 of 7

Frequently asked questions

How many devices does Slenderizers Equipment Mfg., Inc. have in the registry?

The registry currently lists 7 devices for Slenderizers Equipment Mfg., Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Slenderizers Equipment Mfg., Inc.'s devices?

Among its 7 most recently registered devices, Slenderizers Equipment Mfg., Inc. has devices listed in FDA 510(k) (7 devices).

What risk classes do Slenderizers Equipment Mfg., Inc.'s devices fall under?

Among its 7 most recently registered devices, the classes recorded for Slenderizers Equipment Mfg., Inc.'s devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from Slenderizers Equipment Mfg., Inc. in the registry?

The most recently registered devices listed for Slenderizers Equipment Mfg., Inc. include MULTI-FLEX TABLE -- MODEL 102, MULTI-FLEX TABLE -- MODEL 101, MULTI-FLEX TABLE -- MODEL 103 and MULTI-FLEX TABLE -- MODEL 105.

Generated automatically from registry data and not verified by a human reviewer.