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Rapid Reboot SP-H1

by Rapid Reboot Recovery Products

Rapid Reboot SP-H1 is an intermittent venous compression system (FDA Class II; FDA product code IRP, Massager, Powered Inflatable Tube) made by Rapid Reboot Recovery Products, listed in FDA GUDID since 10 Jan 2019 (UDI-DI B691SPH10), registry data as of 23 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 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing NumberB691SPH10 UDI-DI Date10 Jan 2019ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade name
Rapid Reboot
Generic name
Intermittent venous compression system
Model / reference
SP-H1
Primary DI / UDI-DI
B691SPH10
FDA product code
IRP
GMDN term
Intermittent venous compression system
Device class
Class II
Regulation number
890.5650
GUDID distribution status
In Commercial Distribution

Related devices

Category: Intermittent venous compression systemSequential venous compression system

Similar devices

Other devices filed under FDA product code IRP (Massager, Powered Inflatable Tube).

Other devices from Rapid Reboot Recovery Products

See all devices from Rapid Reboot Recovery Products →

Properties

  • Prescription use
  • Over-the-counter
  • Lot / batch number
Other properties (12, all answered No)