Home › Device types › LMG
Agent, Absorbable Hemostatic, Non-Collagen Based
FDA product code LMG · Class 3 · General, Plastic Surgery
51
Registered devices
1,755
Adverse events
4
Recalls
0
510(k) clearances
Devices with this code
SURGICEL NU-KNIT — Ethicon SàrlARISTA — Davol Inc.PerClot — BAXTER HEALTHCARE CORPORATIONSURGICEL NU-KNIT — Ethicon SàrlSURGICEL — Ethicon SàrlSURGICEL NU-KNIT — Ethicon SàrlSURGICEL FIBRILLAR — Ethicon SàrlEmergency Medical Products — EMERGENCY MEDICAL PRODUCTS, INC.Veriset — Covidien LPSURGICEL NU-KNIT — Ethicon SàrlSURGICEL SNoW — ETHICON, LLCARISTA — Davol Inc.SURGICEL NU-KNIT — Ethicon SàrlSURGICEL FIBRILLAR — Ethicon SàrlSURGICEL FIBRILLAR — ETHICON, LLCSURGICEL — Ethicon SàrlARISTA — Davol Inc.SURGICEL — Ethicon SàrlVeriset — Covidien LPSURGICEL — Ethicon SàrlSURGICEL FIBRILLAR — ETHICON, LLCSURGICEL NU-KNIT — Ethicon SàrlSURGICEL FIBRILLAR — ETHICON, LLCEmergency Medical Products — EMERGENCY MEDICAL PRODUCTS, INC.
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2025-11-03 | GET TESTED INTERNATIONAL AB | Distribution without premarket approval/clearance. |
| 2025-11-03 | GET TESTED INTERNATIONAL AB | Distribution without premarket approval/clearance. |
| 2024-06-11 | Ethicon Sarl, a Johnson & Johnson Company | Some foil pouches were found torn open, impacting the sterile barrier which was traced to a specific machine used during product packaging. |
| 2024-06-11 | Ethicon Sarl, a Johnson & Johnson Company | Some foil pouches were found torn open, impacting the sterile barrier which was traced to a specific machine used during product packaging. |
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