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Device Explorer · FDA GUDID · GMDN 40126

Metacarpal prosthesis

A sterile implantable device designed to replace the proximal end (base) of the first metacarpal of the thumb carpometacarpal (CMC) joint (articulation with the trapezium) typically to treat thumb instability/motion disabilities caused by arthritis or fracture

US‑registered devices124in commercial distribution
Companies7labelers on GUDID
Single‑use48%of device records
Sterile48%labelled sterile
Prescription100%Rx‑only share
ImplantableYesGMDN flag
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Share of device records

Skeletal Dynamics L.L.C.6351%
Keri Medical Sa1613%
Ascension Orthopedics, Inc.1411%
Smith & Nephew, Inc.1210%
Ensemble Orthopedics, Inc.1210%
Wright Medical Technology, Inc.54%
Parcus Medical Llc22%

Top labelers

CompanyDevicesShare
Skeletal Dynamics L.L.C.6351%
Keri Medical Sa1613%
Ascension Orthopedics, Inc.1411%
Smith & Nephew, Inc.1210%
Ensemble Orthopedics, Inc.1210%
Wright Medical Technology, Inc.54%
Parcus Medical Llc22%

Company = labeler of record on GUDID. 7 companies in total; top 12 shown. Click headers to sort.

Brand names on the register (sample)

NuGrip CMCMCP SystemPyroSphere CMCStablyxSWANSONATLASEnsemble CMCAscension® NuGrip®Ascension® PyroSphereTOUCH® CMC 1

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

FDA product codes

CodeNameDevices
KYIPROSTHESIS, WRIST, CARPAL TRAPEZIUM60
HSBROD, FIXATION, INTRAMEDULLARY AND ACCESSORIES22
SFAProsthesis, Finger, Semi-Constrained, Metal/Polymer16
KYIProsthesis, Wrist, Carpal Trapezium12
KYIProsthesis, wrist, carpal trapezium10
KWDPROSTHESIS, TOE, HEMI-, PHALANGEAL5

GMDN & GCC registration

  • GMDN code 40126 · implantable
  • Single‑use 48% · sterile 48% · Rx‑only 100% · 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.

No closely related category with 50+ devices.

How many metacarpal prosthesis products are registered in the US?

124 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Metacarpal prosthesis", from 7 companies. The largest labeler is Skeletal Dynamics L.L.C. with 51% of records.

Which FDA product codes apply?

KYI (PROSTHESIS, WRIST, CARPAL TRAPEZIUM), HSB (ROD, FIXATION, INTRAMEDULLARY AND ACCESSORIES), SFA (Prosthesis, Finger, Semi-Constrained, Metal/Polymer), KYI (Prosthesis, Wrist, Carpal Trapezium)

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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