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Squid Wrist

by Portable Therapeutix

Squid Wrist is a Class I device made by Portable Therapeutix, listed in FDA GUDID since 6 Jul 2016 (UDI-DI 00811107020156), 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 Number00811107020156 UDI-DI Date6 Jul 2016ListedStatusListed 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  • Withdrawn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
Generic name
Inflatable hot/cold therapy pack/electric pump
Model / reference
Wrist
Primary DI / UDI-DI
00811107020156
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, Reuseable).

Other devices from Portable Therapeutix

See all devices from Portable Therapeutix →

Properties

  • Over-the-counter
  • Convenience kit
Other properties (13, all answered No)