510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K871296Substantially Equivalent

T.e.d.(tm) Traction Device

The Kendal Co., Boston MA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K871296 is the FDA 510(k) clearance record for T.E.D.(TM) TRACTION DEVICE, a class I device, cleared for The Kendal Co. on under FDA product code KQZ (Component, Traction, Non-Invasive). FDA records list 63 510(k) clearances for The Kendal Co., from to . As of , FDA records show no recalls naming K871296.

Clearance record

Decision date
Received
(15 days to decision)
Product code
KQZ Component, Traction, Non-Invasive
Regulation
21 CFR 888.5890
Device class
Class I
Review panel
Orthopedic
Applicant
The Kendal Co. One Federal St., Boston MA
Third party review
No

Clearances, product code KQZ

Trailing 12 months

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

FDA records show no clearances under product code KQZ in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code KQZ, 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