Medical Device Manufacturer · US , Puyallup , WA

Stl International, Inc.

1 submissions · 1 cleared · Since 2016

Total

Cleared

Denied

Stl International, Inc. — FDA 510(k) Submissions

Stl International, Inc. has submitted 1 FDA 510(k) premarket notifications since 2016, of which 1 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Apparatus, Traction, Non-powered . Use the specialty filter in the sidebar to narrow results.

1 devices

1–1 of 1

Teeter Manual Inversion Table; Teeter Gravity Boots; Teeter Forward Rotation Decompression Device; Teeter Portable Decompression Device; Teeter Horizontal Decompression Table

K162702 · HST Apparatus, Traction,... · Neurology

Dec 2016 93d

Stl International, Inc.

Stl International, Inc. — FDA 510(k) Submissions

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