Surgical Appliance Industries, Inc.

Surgical Appliance Industries, Inc. — FDA 510(k) Submissions

Surgical Appliance Industries, Inc. has submitted 9 FDA 510(k) premarket notifications since 1981, of which 9 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Orthosis, Lumbo-sacral, Joint, Knee, External Brace, Stocking, Medical Support (to Prevent Pooling Of Blood In Legs), Orthosis, Limb Brace, Orthosis, Thoracic . Use the specialty filter in the sidebar to narrow results.