Home › Device types › LYY
Latex Patient Examination Glove
FDA product code LYY · Class 1 · General Hospital
1,647
Registered devices
2,992
Adverse events
6
Recalls
1,954
510(k) clearances
Devices with this code
Safco DuraSoft Latex Gloves — SAFCO DENTAL SUPPLY CO.AMMEX Professional — AMMEX CORPORATIONThe Orthodontic Store — Young Innovations, Inc.Criterion PC Glove PF Latex — HENRY SCHEIN, INC.Pure Grip G2 — HENRY SCHEIN, INC.Advance Dental Products — The Atlanta Dental Supply CompanyLatex Exam XS PF Txt Gloves (100) — BURKHART DENTAL SUPPLY CO., THEMEDHANDLER — Foodhandler Inc.BioSkin — LIBERTY GLOVE & SAFETY, LLCAMBITEX — Cardinal Health 200, LLCMICROFLEX — Ansell Healthcare ProductMidway Select — MIDWAY DENTAL SUPPLY, LLCMICROFLEX — Ansell Healthcare ProductNipro Latex Examination Gloves — NIPRO MEDICAL CORPORATIONDermatec Viper Latex — Relda, Llc.Gen-X® — SMART GLOVE INTERNATIONAL PTE. LTD.SkinGard TPF — MARCON RUBBER INDUSTRY SDN BHDProWorks — TRANZONIC COMPANIES, THESaf-Care Plus — ECON DISPOSABLE SUPPLIES, INCDental City — ICP, INC.PINK RIBBON LATEX PF EXAM PNK VT BX MD — Smarthealth, Inc.AloePRO™ — Dash Medical Gloves, Inc.AURELIA VIBRANT — SUPERMAX GLOVE MANUFACTURING SDN. BHD.Precision Grip Nitrile Exam Gloves — Total Source Manufacturing
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2020-08-19 | Ansell Healthcare Products LLC | Examination gloves were shipped inadvertently, without to verify barrier integrity. |
| 2011-12-22 | Adenna Inc | The recall was initiated because Adenna Inc. distributed latex gloves that have been FDA refused. |
| 2006-04-10 | Gulf South Medical Supply Inc | FDA's laboratory analysis found holes in the gloves that exceeded the allowable limit. Gloves with holes compromise the integrity of the latex barrier and have |
| 2003-06-27 | Henry Schein, Inc. | FDA's analysis revealed defects (holes) in the latex gloves. |
| 2003-06-27 | Henry Schein, Inc. | FDA's analysis revealed defects (holes) in the latex gloves. |
| 2002-07-23 | American Healthcare Products Inc | Unfit for intended use due to stickiness. |
Query this across every FDA database — by API.
Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.
Get your free API keyRead the docsSourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.