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Recovery+ Go Ankle Thermal Compression Wrap RP-2000AW

by Wmi Enterprises, LLC

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

None found

in data synced 22 Oct 2026

Documents

None

No authorization documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source GUDID, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00850087597067 UDI-DI Date23 Jul 2026ListedStatusListed GUDID: in commercial distribution

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 22 Oct 2026.

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade Name
Recovery+ Go Ankle Thermal Compression Wrap
Generic Name
Inflatable hot/cold therapy pack/electric pump
Model / Reference
RP-2000AW
Primary DI / UDI-DI
00850087597067
510(k) Number
FDA Product Code
IME
GMDN Term
Inflatable hot/cold therapy pack/electric pump
Device Class
Class I
Regulation Number
890.5700
GUDID distribution status
In Commercial Distribution

Related devices

Cleared under the same submission (K253076)

Other devices from Wmi Enterprises, LLC

See all devices from Wmi Enterprises, LLC →

Properties

  • Single Use
  • Prescription Use
  • Lot / Batch Number
  • Serial Number
  • Manufacturing Date

Other properties (9)

  • Sterile: No
  • Implantable: No
  • Contains Latex: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Expiration Date: No