510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K123829Substantially Equivalent

Portable Therapeutix Squid Active Cold Compression Device and Cold Pack

Portable Therapeutix, Ashland MA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K123829 is the FDA 510(k) clearance record for PORTABLE THERAPEUTIX SQUID ACTIVE COLD COMPRESSION DEVICE AND COLD PACK, a class II device, cleared for Portable Therapeutix, LLC on under FDA product code IRP (Massager, Powered Inflatable Tube). FDA records list 2 510(k) clearances for Portable Therapeutix, LLC, from to . As of , FDA records show no recalls naming K123829.

Clearance record

Decision date
Received
(112 days to decision)
Product code
IRP Massager, Powered Inflatable Tube
Regulation
21 CFR 890.5650
Device class
Class II
Review panel
Physical Medicine
Applicant
Portable Therapeutix, LLC 200 Homer Ave., Ashland MA
510(k) summary
Summary PDF
Third party review
No

Clearances, product code IRP

Trailing 12 months
11 clearances under product code IRP in the twelve months to October 2026, April 2026 the highest month at 3.
Show the numbers
Monthly 510(k) clearances under FDA product code IRP, trailing twelve months
MonthClearances
November 20251
December 20250
January 20261
February 20260
March 20260
April 20263
May 20262
June 20261
July 20262
August 20261
September 20260
October 20260