Activator V-E
by Activator Methods International, Ltd.
510(k) K112606
Activator V-E is a medical device (FDA unclassified; FDA product code LXM, Manipulator, Plunger-Like Joint) made by Activator Methods International, Ltd., cleared under FDA 510(k) K112606 on 6 Mar 2012, active as of 10 Oct 2026.
Active
510(k)
Valid until
No expiry
FDA recalls
None found
Documents
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | FDA 510(k)SESE | NumberK112606 | Date6 Mar 2012 | StatusActive |
Official records
- FDA 510(k) database K112606
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- 510(k) Number
- FDA product code
- LXM
- Device class
- U
- Advisory committee
- Unknown
- FDA decision
- SESE Substantially Equivalent
Similar devices
Other devices filed under FDA product code LXM (Manipulator, Plunger-Like Joint).
- MAX ADJUSTING INSTRUMENT by Manna Omni International, Inc.
- ATLAS ORTHOGONAL PERCUSSION INSTTUMENT by Sweat Chiropractic Clinic
- KINETIC TECHNOLOGY PRECISION ADJUSTOR MOD. SHLCP-5 by Kinetic Technology, Inc.
- KINETIC TECHNOOGY PRECISION ADJUSTOR MODEL SHLCP-1 by Kinetic Technology, Inc.
- KHAN KINETIC TREATMENT DEVICE (KKT-M1) by Optima Health Solutions International, Inc.
- JTECH ADJUSTER REFLEX GUN by J-Tech Medical, Inc.
- TORQUE INSTRUMENT, MODEL 8500 by Spinalight, Inc.
- IMPULSE IQ ADJUSTING INSTRUMENT by NEUROMECHANICAL INNOVATIONS, LLC
- VSTAAR AdjusteR by Spinal Acoustics, LLC
- Atlas Percussion Adjusting Instrument by Spinalight, Inc.