510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K162702Substantially Equivalent

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

STL International, Inc., Puyallup WA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K162702 is the FDA 510(k) clearance record for Teeter Manual Inversion Table; Teeter Gravity Boots; Teeter Forward Rotation Decompression Device; Teeter Portable Decompression Device; Teeter Horizontal Decompression Table, a class I device, cleared for Stl International, Inc. on under FDA product code HST (Apparatus, Traction, Non-Powered). FDA records list one 510(k) clearance for Stl International, Inc. As of , FDA records show no recalls naming K162702.

Clearance record

Decision date
Received
(93 days to decision)
Product code
HST Apparatus, Traction, Non-Powered
Regulation
21 CFR 888.5850
Device class
Class I
Review panel
Orthopedic
Applicant
Stl International, Inc. 9902 162nd St., Ct. E, Puyallup WA
510(k) summary
Summary PDF
Third party review
No

Clearances, product code HST

Trailing 12 months

FDA records hold no clearances under product code HST in the trailing twelve months.

FDA records show no clearances under product code HST in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code HST, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260