A device used during a medical/surgical procedure to steadily hold a patient's foot (feet) by cradling the heel. It is typically attached to an operating table, examination table, or treatment chair and is considered an accessory to these devices. This device
| Company | Devices | Share |
|---|---|---|
| Hill-Rom, Inc. | 47 | 44% |
| Schuerch Corporation | 40 | 37% |
| Steris Corporation | 6 | 6% |
| United Metal Fabricators, Inc. | 5 | 5% |
| Qfix | 4 | 4% |
| Mid Central Medical Corp. | 3 | 3% |
| Orthopediatrics Corp. | 1 | 1% |
| Bird & Cronin, Llc | 1 | 1% |
| David Scott Company | 1 | 1% |
Company = labeler of record on GUDID. 9 companies in total; top 12 shown. Click headers to sort.
Sample of brand names as labelled; no endorsement. Ask us for the full list with company, model and UDI.
| Code | Name | Devices |
|---|---|---|
| FWZ | Operating Room Accessories Table Tray | 98 |
| EYD | Stirrups | 9 |
| EYD | STIRRUPS | 6 |
| IZI | System, X-Ray, Angiographic | 4 |
| JAK | System, X-Ray, Tomography, Computed | 4 |
| KPS | System, Tomography, Computed, Emission | 4 |
Use these as the dimensions to specify in a tender line.
108 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Heel stirrup", from 9 companies. The largest labeler is Hill-Rom, Inc. with 44% of records.
FWZ (Operating Room Accessories Table Tray), EYD (Stirrups), EYD (STIRRUPS), IZI (System, X-Ray, Angiographic)
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.
Add heel stirrup to the RFQ basket or use the form below with quantity, specification and delivery location; the Network returns comparable quotes from verified suppliers in 2–5 working days.
Hospitals, pharmacies and distributors anywhere: tell us what you need and the Consulting Wallah Network returns comparable quotes from verified suppliers. No fee for buyers.
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.