A sterile non-bioabsorbable device made of metal and/or metal oxide [e.g., titanium (Ti)] implanted into the body to provide osteoconductive bone-tissue scaffolds to replace maxillofacial and/or mandibular bone lost through trauma or dental surgery. It is typi
| Company | Devices | Share |
|---|---|---|
| Integrated Dental Systems, Llc | 111 | 85% |
| Megagen Implant Co. Ltd | 12 | 9% |
| Unicare Biomedical Inc. | 5 | 4% |
| Osteogenics Biomedical Inc | 2 | 2% |
Company = labeler of record on GUDID. 4 companies in total; top 12 shown. Click headers to sort.
Sample of brand names as labelled; no endorsement. Ask us for the full list with company, model and UDI.
| Code | Name | Devices |
|---|---|---|
| DZE | Implant, Endosseous, Root-Form | 111 |
| JEY | Plate, Bone | 19 |
Use these as the dimensions to specify in a tender line.
130 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Dental bone matrix implant, metallic", from 4 companies. The largest labeler is Integrated Dental Systems, Llc with 85% of records.
DZE (Implant, Endosseous, Root-Form), JEY (Plate, Bone)
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.