Consulting Wallah › Device Explorer › Other devices › Synovial fluid supplementation medium
Device Explorer · FDA GUDID · GMDN 44757

Synovial fluid supplementation medium

A sterile viscous/elastic solution or gel (e.g., comprised of hyaluronic acids and their polymeric derivatives) intended to be injected into joints (particularly large, load-bearing joints such as the hip or knee) to help cushion the joint, especially in cases

US‑registered devices95in commercial distribution
Companies24labelers on GUDID
Single‑use100%of device records
Sterile100%labelled sterile
Prescription99%Rx‑only share
ImplantableYesGMDN flag
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Share of device records

Fcl Health Solutions Ltd88%
Acre Pharma Limited77%
Ally Medical Supplies Ltd77%
Nuvara Srl77%
Maplestone Developments Limited66%
Pavan Trading Ltd66%
Fidia Farmaceutici Spa66%
Propharma-Uk Ltd55%

Top labelers

CompanyDevicesShare
Fcl Health Solutions Ltd88%
Acre Pharma Limited77%
Ally Medical Supplies Ltd77%
Nuvara Srl77%
Maplestone Developments Limited66%
Pavan Trading Ltd66%
Fidia Farmaceutici Spa66%
Propharma-Uk Ltd55%
Pharmaceutical Health Limited55%
Pharmamondis Gmbh55%
Saima Global Farma S.L.55%
Anika Therapeutics, Inc.44%

Company = labeler of record on GUDID. 24 companies in total; top 12 shown. Click headers to sort.

Brand names on the register (sample)

SynviscOrthoviscMonoviscEuflexxaDurolaneSynvisc OneSupartzSynvisc One (Synvisc Three)HyalganRadiesseVISCO-3 sodium hyaluronateGel-One® Cross-linked HyaluronateArthrex®TriVisc®GenVisc® 850TriVisc™ sodium hyaluronate

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

FDA product codes

CodeNameDevices
MOZAcid, Hyaluronic, Intraarticular112
MOZAcid, hyaluronic, intraarticular9
PKYImplant, Dermal, For Aesthetic Use In The Hands1
LMHImplant, Dermal, For Aesthetic Use1

GMDN & GCC registration

  • GMDN code 44757 · implantable
  • Single‑use 100% · sterile 100% · 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

Total Volume (Milliliter) · 10

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

No closely related category with 50+ devices.

How many synovial fluid supplementation medium products are registered in the US?

95 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Synovial fluid supplementation medium", from 24 companies. The largest labeler is Fcl Health Solutions Ltd with 8% of records.

Which FDA product codes apply?

MOZ (Acid, Hyaluronic, Intraarticular), MOZ (Acid, hyaluronic, intraarticular), PKY (Implant, Dermal, For Aesthetic Use In The Hands), LMH (Implant, Dermal, For Aesthetic Use)

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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