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Device Explorer · FDA GUDID · GMDN 33178

Revision uncoated hip femur prosthesis

A sterile device designed to replace the entire femoral component of a total hip prosthesis implanted during replacement of the total hip prosthesis typically due to wear. The revision device is composed of two or more separate segments (e.g., femoral head, ne

US‑registered devices407in commercial distribution
Companies6labelers on GUDID
Single‑use99%of device records
Sterile99%labelled sterile
Prescription99%Rx‑only share
ImplantableYesGMDN flag
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Share of device records

Zimmer, Inc.12330%
Zimmer Gmbh10526%
Exactech, Inc.8822%
Waldemar Link Gmbh & Co. Kg6616%
Corin Ltd133%
Encore Medical, L.P.123%

Top labelers

CompanyDevicesShare
Zimmer, Inc.12330%
Zimmer Gmbh10526%
Exactech, Inc.8822%
Waldemar Link Gmbh & Co. Kg6616%
Corin Ltd133%
Encore Medical, L.P.123%

Company = labeler of record on GUDID. 6 companies in total; top 12 shown. Click headers to sort.

Brand names on the register (sample)

MP Reconstruction ProsthesisMegasystem CSPII Model LubinusWagner SL Revision®Wagner Cone Prosthesis®ZMR®NAVerSys®VerSys Heritage®DJO SURGICALAlteonRevival Modular Hip Stem

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

FDA product codes

CodeNameDevices
LZOProsthesis, hip, semi-constrained, metal/ceramic/polymer, ce197
JDIProsthesis, hip, semi-constrained, metal/polymer, cemented187
LPHPROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNC132
KWZProsthesis, hip, constrained, cemented or uncemented, metal/123
LZOProsthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Ce119
LWJProsthesis, hip, semi-constrained, metal/polymer, uncemented86

GMDN & GCC registration

  • GMDN code 33178 · implantable
  • Single‑use 99% · sterile 99% · Rx‑only 99% · 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

Outer Diameter (Millimeter) · 129Length (Millimeter) · 127Angle (degree) · 13Height (Millimeter) · 6

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

How many revision uncoated hip femur prosthesis products are registered in the US?

407 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Revision uncoated hip femur prosthesis", from 6 companies. The largest labeler is Zimmer, Inc. with 30% of records.

Which FDA product codes apply?

LZO (Prosthesis, hip, semi-constrained, metal/ceramic/polymer, ce), JDI (Prosthesis, hip, semi-constrained, metal/polymer, cemented), LPH (PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNC), KWZ (Prosthesis, hip, constrained, cemented or uncemented, metal/)

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.

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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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