BTE Dynamic Lift

No FDA recalls found in the data synced 22 Oct 2026.

Full name

The Bte Dynamic Lift

510(k) Number

K924414 ↗

FDA Product Code

IKK

Device Class

Class II

Regulation

21 CFR Part 890.1925

Advisory Committee

Physical Medicine

FDA Decision

SESE Substantially Equivalent

• The Bte Vector; Analysis System for the Low Back

  Class I

  FDA 510(k) K925225 Active Cleared 27 Jun 1994

• Bte Cpm-20

  Class I

  FDA 510(k) K955106 Active Cleared 29 Dec 1995

• Bte Cpm-10

  Class I

  FDA 510(k) K955105 Active Cleared 29 Dec 1995

• Motionspect

  Class III

  FDA 510(k) K895881 Active Cleared 10 Apr 1990

• The Bte WS30

  Class II

  FDA 510(k) K933611 Active Cleared 20 Jun 1994

• Work Simulator

  Class I

  FDA 510(k) K800007 Active Cleared 21 Jan 1980

• What is the BTE Dynamic Lift used for?

  The BTE Dynamic Lift is a system for isokinetic testing and evaluation used in physical medicine. It provides functional rehabilitation capabilities for therapeutic purposes in clinical settings.

• What is the regulatory status of the BTE Dynamic Lift?

  The BTE Dynamic Lift is authorized under FDA 510K clearance K924414. It is a Class II device with product code IKK and is used in physical medicine settings.

• Who manufactures the BTE Dynamic Lift?

  The BTE Dynamic Lift is manufactured by Baltimore Therapeutic Equipment Co., located in Hanover, MD. The company has been producing this device since it received FDA clearance in 1993.

• What is the BTE Dynamic Lift classified as?

  The BTE Dynamic Lift is classified as a Class II medical device with product code IKK. It is specifically designed for isokinetic testing and evaluation in physical medicine applications.