A device made of Hevea natural rubber latex (NRL) intended as a protective barrier when worn on the hands of healthcare providers during patient examination/treatment or for other sanitary purposes; its inner surface is not covered with powder and it does not
| Company | Devices | Share |
|---|---|---|
| Henry Schein, Inc. | 158 | 10% |
| Ansell Healthcare Product | 80 | 5% |
| Smarthealth, Inc. | 50 | 3% |
| Mexpo International Inc. | 49 | 3% |
| Mckesson Medical-Surgical Inc. | 48 | 3% |
| Innovative Healthcare Corporation | 44 | 3% |
| Econ Disposable Supplies, Inc | 40 | 2% |
| Uline, Inc. | 40 | 2% |
| Top Quality Manufacturing, Inc. | 36 | 2% |
| Uniseal | 34 | 2% |
| Ascend Eagle Incorporated | 34 | 2% |
| Liberty Glove & Safety, Llc | 30 | 2% |
Company = labeler of record on GUDID. 124 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 |
|---|---|---|
| LYY | Latex Patient Examination Glove | 1,227 |
| LYY | Latex patient examination glove | 361 |
| LZA | Polymer Patient Examination Glove | 83 |
| LZC | Medical Glove, Specialty | 58 |
| LZC | Patient Examination Glove, Specialty | 45 |
| LYZ | Vinyl Patient Examination Glove | 11 |
Use these as the dimensions to specify in a tender line.
1,656 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Hevea-latex examination/treatment glove, non-powdered, non-antimicrobial", from 124 companies. The largest labeler is Henry Schein, Inc. with 10% of records.
LYY (Latex Patient Examination Glove), LYY (Latex patient examination glove), LZA (Polymer Patient Examination Glove), LZC (Medical Glove, Specialty)
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.