A small device designed to be used during a surgical procedure to make a physical connection between two orthopaedic instruments, instrument components, or an orthopaedic instrument and another device (e.g., an implant) to facilitate the insertion and placemen
| Company | Devices | Share |
|---|---|---|
| Life Spine, Inc. | 98 | 11% |
| Djo, Llc | 67 | 8% |
| Osteocentric Technologies, Inc. | 64 | 7% |
| Synthes Gmbh | 57 | 7% |
| Biomet Orthopedics, Llc | 55 | 6% |
| Medtronic Sofamor Danek, Inc. | 41 | 5% |
| Encore Medical, L.P. | 40 | 5% |
| Captiva Spine, Inc. | 32 | 4% |
| Orthopediatrics Canada Ulc | 29 | 3% |
| Altus Spine, Llc | 28 | 3% |
| Advanced Orthopaedic Solutions, Inc. | 24 | 3% |
| Highridge Medical, Llc | 23 | 3% |
Company = labeler of record on GUDID. 65 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 |
|---|---|---|
| LXH | Orthopedic manual surgical instrument | 216 |
| MNH | Orthosis, Spondylolisthesis Spinal Fixation | 189 |
| MNI | Orthosis, Spinal Pedicle Fixation | 189 |
| LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT | 146 |
| LXH | Orthopedic Manual Surgical Instrument | 97 |
| NKB | Orthosis, Spinal Pedicle Fixation, For Degenerative Disc Dis | 51 |
Use these as the dimensions to specify in a tender line.
862 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Orthopaedic instrument surgical connector", from 65 companies. The largest labeler is Life Spine, Inc. with 11% of records.
LXH (Orthopedic manual surgical instrument), MNH (Orthosis, Spondylolisthesis Spinal Fixation), MNI (Orthosis, Spinal Pedicle Fixation), LXH (ORTHOPEDIC MANUAL SURGICAL INSTRUMENT)
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.