510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K213097Substantially Equivalent

Armory Motion

Pain Management Technologies, Akron OH / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K213097 is the FDA 510(k) clearance record for Armory Motion, a class II device, cleared for Pain Management Technologies, Inc. on under FDA product code ILO (Pack, Hot Or Cold, Water Circulating). FDA records list 6 510(k) clearances for Pain Management Technologies, Inc., from to . As of , FDA records show no recalls naming K213097.

Clearance record

Decision date
Received
(259 days to decision)
Product code
ILO Pack, Hot Or Cold, Water Circulating
Regulation
21 CFR 890.5720
Device class
Class II
Review panel
Physical Medicine
Applicant
Pain Management Technologies, Inc. 1760 Wadsworth Rd., Akron OH
510(k) summary
Summary PDF
Third party review
No

Clearances, product code ILO

Trailing 12 months

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

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