510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
K973506Substantially Equivalent

Activator II

Activator Methods, Inc., Phoenix AZ / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K973506 is the FDA 510(k) clearance record for ACTIVATOR II, cleared for Activator Methods, Inc. on under FDA product code LXM (Manipulator, Plunger-Like Joint). FDA records list one 510(k) clearance for Activator Methods, Inc. As of , FDA records show no recalls naming K973506.

Clearance record

Decision date
Received
(133 days to decision)
Product code
LXM Manipulator, Plunger-Like Joint
Device class
Unclassified
Review panel
Unknown
Applicant
Activator Methods, Inc. 3714 E. Indian School Rd., Phoenix AZ
510(k) summary
Summary
Third party review
No

Clearances, product code LXM

Trailing 12 months

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

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