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Squid Rx Left Shoulder

by Portable Therapeutix

Squid Rx Left Shoulder is a Class I device made by Portable Therapeutix, listed in FDA GUDID since 21 Jul 2023 (UDI-DI 00811107020903), registry data as of 22 Oct 2026.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Source GUDID, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00811107020903 UDI-DI Date21 Jul 2023ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name
Squid Rx
Generic name
Inflatable hot/cold therapy pack/electric pump
Model / reference
Left Shoulder
Primary DI / UDI-DI
00811107020903
FDA product code
IME, IRP
GMDN term
Inflatable hot/cold therapy pack/electric pump
Device class
Class I
Regulation number
890.5700, 890.5650
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code IME (Pack, Hot Or Cold, Reusable).

Other devices from Portable Therapeutix

See all devices from Portable Therapeutix →

Properties

  • Prescription use
  • Convenience kit
Other properties (13, all answered No)