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Device Explorer · FDA GUDID · GMDN 61780

Acetabular augmentation implant

A sterile implantable device intended to help prevent dislocation of a total hip replacement by augmenting the posterior lip of the acetabulum around a retained acetabular prosthesis, or to help fill bone defects not covered by the acetabular prosthesis. It is

US‑registered devices144in commercial distribution
Companies5labelers on GUDID
Single‑use100%of device records
Sterile100%labelled sterile
Prescription100%Rx‑only share
ImplantableYesGMDN flag
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Share of device records

Medacta International Sa4934%
Smith & Nephew, Inc.4128%
Waldemar Link Gmbh & Co. Kg2618%
Depuy (Ireland)2417%
Maxx Orthopedics, Inc.43%

Top labelers

CompanyDevicesShare
Medacta International Sa4934%
Smith & Nephew, Inc.4128%
Waldemar Link Gmbh & Co. Kg2618%
Depuy (Ireland)2417%
Maxx Orthopedics, Inc.43%

Company = labeler of record on GUDID. 5 companies in total; top 12 shown. Click headers to sort.

Brand names on the register (sample)

TrabecuLink AugmentsREDAPTFREEDOM STEMMEDPINNACLE GRIPTIONMpact 3D Metal Augments II

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

FDA product codes

CodeNameDevices
LPHPROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNC114
MEHProsthesis, Hip, Semi-Constrained, Uncemented, Metal / Polym26
LPHProsthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Unc26
LZOProsthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Ce26
JWHPROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEM24
KROPROSTHESIS, KNEE, FEMOROTIBIAL, CONSTRAINED, CEMENTED, METAL24

GMDN & GCC registration

  • GMDN code 61780 · implantable
  • Single‑use 100% · sterile 100% · 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.

How many acetabular augmentation implant products are registered in the US?

144 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Acetabular augmentation implant", from 5 companies. The largest labeler is Medacta International Sa with 34% of records.

Which FDA product codes apply?

LPH (PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNC), MEH (Prosthesis, Hip, Semi-Constrained, Uncemented, Metal / Polym), LPH (Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Unc), LZO (Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Ce)

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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