Home › Device types › NAC
Dressing, Wound, Hydrophilic
FDA product code NAC · Class 1 · General, Plastic Surgery
2,327
Registered devices
1,397
Adverse events
9
Recalls
4
510(k) clearances
Devices with this code
Zeni Medical — Focus Health Group, Inc.Henry Schein — HENRY SCHEIN, INC.AMD-RITMED — AMD Medicom IncDr.Med — Roosin Medical Co., Ltd.Dukal — Dukal LLCDeRoyal — DEROYAL INDUSTRIES, INC.ProCure — Twin Med, LLCMedifoam H band large — Genewel Co.,Ltd.Sequa® Sorb — Foshan United Medical Technologies Ltd.AQUACEL EXTRA — CONVATEC, PURCHASING DEPARTMENTMedline — MEDLINE INDUSTRIES, INC.EXU-DRY PaD 24X36IN NONPR PK24 — SMITH & NEPHEW MEDICAL LIMITEDCutimed® Sorbion® — BSN medical GmbHCovaWound™ Alginate 15x20 — Covalon Technologies LtdDeRoyal — DEROYAL INDUSTRIES, INC.Simpurity — SAFE N' SIMPLE LLC3M™ Tegaderm™ — 3M COMPANYDeRoyal — DEROYAL INDUSTRIES, INC.DeRoyal — DEROYAL INDUSTRIES, INC.AMD-RITMED ALL GAUZE — AMD Medicom IncWalgreens — WALGREEN CO.Cutimed® — BSN medical GmbHSequa® Cel — Foshan United Medical Technologies Ltd.DryMax FOAM — Absorbest AB
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2026-05-18 | DeRoyal Industries Inc | Sterile wound dressing, lacks sterility assurance |
| 2025-02-19 | MEDLINE INDUSTRIES, LP - Northfield | There is a potential for the sterility of the device to be compromised. |
| 2024-10-01 | Advanced Medical Solutions Ltd. | Due to defects on primary packaging pouch that compromise the device's ability to maintain a sterile barrier. |
| 2024-10-01 | Advanced Medical Solutions Ltd. | Due to defects on primary packaging pouch that compromise the device's ability to maintain a sterile barrier. |
| 2024-10-01 | Advanced Medical Solutions Ltd. | Due to defects on primary packaging pouch that compromise the device's ability to maintain a sterile barrier. |
| 2024-02-27 | ConvaTec, Inc | The product does not meet sterility assurance level. |
| 2024-01-23 | MEDLINE INDUSTRIES, LP - Northfield | Product failed sterility testing. |
| 2016-06-08 | Amd-Ritmed, Inc. | The lot of transparent dressing was found to be contaminated (not sterile) based on FDA sampling and analysis. |
| 2004-01-19 | DeRoyal Surgical Tray | Hydrophilic powder wound dressing, sterilized at a dosage which subsequently failed a sterility audit, was distributed. |
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