Device Explorer · FDA GUDID · GMDN 41141

Arm cushion

A soft pillow or pad used to provide support and comfort to the user's arm, typically during the treatment and/or prevention of musculoskeletal or circulatory disorders (e.g., muscle sprain/strain, lymphoedema). The device may be used to support various areas

US‑registered devices62in commercial distribution
Companies4labelers on GUDID
Single‑use6%of device records
Sterile0%labelled sterile
Prescription3%Rx‑only share
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Share of device records

Steris Corporation5792%
Merit Medical Systems, Inc.35%
Schuerch Corporation12%
Deroyal Industries, Inc.12%

Top labelers

CompanyDevicesShare
Steris Corporation5792%
Merit Medical Systems, Inc.35%
Schuerch Corporation12%
Deroyal Industries, Inc.12%

Company = labeler of record on GUDID. 4 companies in total; top 12 shown. Click headers to sort.

Brand names on the register (sample)

RadRest®SchureMedDeRoyalBirkova

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

FDA product codes

CodeNameDevices
LWGSURGICAL TABLE CUSHION57
CCXSUPPORT, PATIENT POSITION4
FWZOperating Room Accessories Table Tray2
LWGSurgical Table Cushion1

GMDN & GCC registration

  • GMDN code 41141 · non‑implantable
  • Single‑use 6% · sterile 0% · Rx‑only 3% · OTC 92%
  • 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 arm cushion products are registered in the US?

62 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Arm cushion", from 4 companies. The largest labeler is Steris Corporation with 92% of records.

Which FDA product codes apply?

LWG (SURGICAL TABLE CUSHION), CCX (SUPPORT, PATIENT POSITION), FWZ (Operating Room Accessories Table Tray), LWG (Surgical Table Cushion)

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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