Consulting Wallah › Device Explorer › Other devices › Hydro-massage turbine
Device Explorer · FDA GUDID · GMDN 14429

Hydro-massage turbine

A mains electricity (AC-powered) device with a motor and impeller designed to be submerged in a water bathtub to aerate and circulate the water (whirlpool effect) for hydrotherapy, typically therapeutic massage for patients with musculoskeletal conditions.

US‑registered devices244in commercial distribution
Companies1labelers on GUDID
Single‑use1%of device records
Sterile0%labelled sterile
Prescription0%Rx‑only share
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Share of device records

Whitehall Manufacturing Co244100%

Top labelers

CompanyDevicesShare
Whitehall Manufacturing Co244100%

Company = labeler of record on GUDID. 1 companies in total; top 12 shown. Click headers to sort.

Brand names on the register (sample)

Whirlpool TurbineWhitehall ThermalatorsWhirlpool TurbineeHydrotherapy WhirlpoolHydrotherapy whirlpool

Sample of brand names as labelled; no endorsement. Ask us for the full list with company, model and UDI.

FDA product codes

CodeNameDevices
ILJBath, Hydro-Massage247

GMDN & GCC registration

  • GMDN code 14429 · non‑implantable
  • Single‑use 1% · sterile 0% · Rx‑only 0% · OTC 93%
  • UAE: MOHAP / DoH medical device registration and an authorised representative are required; Saudi: SFDA MDMA. We check status on request.

Size attributes recorded

No structured size data on the register.

Use these as the dimensions to specify in a tender line.

How many hydro-massage turbine products are registered in the US?

244 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Hydro-massage turbine", from 1 companies. The largest labeler is Whitehall Manufacturing Co with 100% of records.

Which FDA product codes apply?

ILJ (Bath, Hydro-Massage)

Is this the same as UAE/GCC registration?

No. GUDID is the US register. For the UAE (MOHAP/DoH) and Saudi (SFDA/MDMA) a separate registration and a local authorised representative are required; Consulting Wallah can check the status and connect you with registered suppliers.

How do I get quotes?

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Source: FDA AccessGUDID (AccessGUDID full release 2 Nov 2026); counts are device records in commercial distribution grouped by GMDN preferred term; companies are labelers of record. Information only — US listing is not a registration in the UAE or GCC; verify with the regulator. © Consulting Wallah — CC BY‑NC‑ND.

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