Consulting Wallah › Device Explorer › Orthopaedic implants › Hydraulic/pneumatic external ankle-foot prosthesis
Device Explorer · FDA GUDID · GMDN 64724

Hydraulic/pneumatic external ankle-foot prosthesis

A device which is a component of an external lower limb prosthesis designed to functionally replace, in part or total, an absent foot and/or ankle, wherein the principle of operation for dorsiflexion/plantar flexion motion control is based on hydraulics and/or

US‑registered devices702in commercial distribution
Companies1labelers on GUDID
Single‑use0%of device records
Sterile0%labelled sterile
Prescription0%Rx‑only share
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Share of device records

College Park Industries, Inc.702100%

Top labelers

CompanyDevicesShare
College Park Industries, Inc.702100%

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

Brand names on the register (sample)

Odyssey K2Odyssey K3

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

FDA product codes

CodeNameDevices
ISHComponent, External, Limb, Ankle/Foot702

GMDN & GCC registration

  • GMDN code 64724 · non‑implantable
  • Single‑use 0% · sterile 0% · Rx‑only 0% · OTC 0%
  • 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 hydraulic/pneumatic external ankle-foot prosthesis products are registered in the US?

702 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Hydraulic/pneumatic external ankle-foot prosthesis", from 1 companies. The largest labeler is College Park Industries, Inc. with 100% of records.

Which FDA product codes apply?

ISH (Component, External, Limb, Ankle/Foot)

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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