510(K) CLEARANCES 67 ▼8RECALLS POSTED 26CLASS I 2PMA DECISIONS 40 ▼14WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
K940455Substantially Equivalent for Some Indications

Lateral Flexion Machine

Rehab, Inc., Knoxville TN / Traditional, Substantially Equivalent for Some Indications
FDA source (opens on fda.gov)

K940455 is the FDA 510(k) clearance record for LATERAL FLEXION MACHINE, a class I device, cleared for Rehab, Inc. on under FDA product code BXB (Exerciser, Powered). FDA records list one 510(k) clearance for Rehab, Inc. As of , FDA records show no recalls naming K940455.

Clearance record

Decision date
Received
(345 days to decision)
Product code
BXB Exerciser, Powered
Regulation
21 CFR 890.5380
Device class
Class I
Review panel
Physical Medicine
Applicant
Rehab, Inc. P.O. Box 2106, Knoxville TN
Third party review
No

Clearances, product code BXB

Trailing 12 months

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

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