Teeter Manual Inversion Table +4 more— 510(k) K162702

Name: FDA 510(k) clearance K162702
Creator: U.S. Food and Drug Administration
Published: 2016-12-30

Substantially Equivalent

Stl International, Inc.

FDA 510(k) clearance K162702 for Teeter Manual Inversion Table +4 more, Substantially Equivalent on 2016-12-30. Applicant: Stl International, Inc.. Device class: 1.

Clearance details

Device name as filed: Teeter Manual Inversion Table; Teeter Gravity Boots; Teeter Forward Rotation Decompression Device; Teeter Portable Decompression Device; Teeter Horizontal Decompression Table
Applicant: Stl International, Inc.
Product code: Code HST
Device class: Class 1
Regulation: 21 CFR 888.5850
Advisory panel: Orthopedic
Date received: 2016-09-28
Decision date: 2016-12-30
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Puyallup, WA, US

Download summary PDF View on FDA.gov ↗

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Adverse events under product code HST

product code HST

Other: 1
Total: 1

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Data sourced from openFDA. This site is unofficial and independent of the FDA.