A hand-held, line-powered device (which may in addition include a rechargeable battery) that consists of a motorized saw handpiece intended to provide sagittal, oscillating, or reciprocating movement for attachable serrated blades designed to cut through hard/
| Company | Devices | Share |
|---|---|---|
| Suretek Medical | 90 | 82% |
| Smith & Nephew, Inc. | 14 | 13% |
| Osada Electric Co.,Ltd. | 3 | 3% |
| Dentis Co. ,Ltd | 3 | 3% |
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 |
|---|---|---|
| GFA | Blade, Saw, General & Plastic Surgery, Surgical | 91 |
| HAB | SAW, POWERED, AND ACCESSORIES | 15 |
| DZH | SAW, BONE, AC-POWERED | 3 |
| NDP | Accessories, Implant, Dental, Endosseous | 3 |
Use these as the dimensions to specify in a tender line.
110 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Surgical power tool system handpiece, sawing, line-powered", from 4 companies. The largest labeler is Suretek Medical with 82% of records.
GFA (Blade, Saw, General & Plastic Surgery, Surgical), HAB (SAW, POWERED, AND ACCESSORIES), DZH (SAW, BONE, AC-POWERED), NDP (Accessories, Implant, Dental, Endosseous)
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.