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Sign in to claim this brandSmith & Nephew Medical, Ltd.
US
Last updated May 23, 2026
What Smith & Nephew Medical, Ltd. makes
The company manufactures wound care dressings, including non-antimicrobial and antimicrobial absorbent options, hydrophilic-gel exudate-absorbent dressings, adhesive bandages, and medicated wound dressing kits. It also produces negative-pressure wound therapy systems, both electric single-use and battery-powered reusable models, as well as water jet knife handpieces for surgical precision. Additional products include nonadherent wound dressings and specialized dressings like silver-impregnated antimicrobial variants.
The portfolio includes devices classified as Class I, Class II, and unclassified (U) under regulatory frameworks, with listings in the FDA’s Unique Device Identifier (UDI) database. The company operates from the United States, adhering to applicable domestic and international medical device regulations.
Written from this company's registered devices by an AI model, and not verified by a human reviewer.
Frequently asked questions
What types of medical devices does Smith & Nephew Medical, Ltd. primarily manufacture?
Smith & Nephew Medical, Ltd. specializes in wound care solutions, including a variety of dressings such as non-antimicrobial and antimicrobial exudate-absorbent options, hydrophilic-gel dressings, adhesive bandages, and medicated wound dressing kits. They also produce negative-pressure wound therapy systems—both electric single-use and battery-powered reusable models—as well as precision surgical tools like water jet knife handpieces. These devices are designed to address exudate management, wound healing, and surgical precision.
Where is Smith & Nephew Medical, Ltd. based, and how does this affect its regulatory compliance?
Smith & Nephew Medical, Ltd. is based in the United States, which means its devices must comply with U.S. regulatory requirements, including those set by the FDA. As a U.S.-based manufacturer, its products are subject to FDA oversight, including classification under Class I, Class II, or unclassified (U) categories, and mandatory listing in the FDA’s Unique Device Identifier (UDI) database to ensure traceability and regulatory transparency.
Which regulatory registries or databases list Smith & Nephew Medical, Ltd.’s devices?
Smith & Nephew Medical, Ltd.’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. This registry ensures standardized identification and tracking of medical devices, facilitating compliance, recall management, and post-market surveillance. The UDI system helps healthcare providers, regulators, and manufacturers maintain accurate records of device performance and safety.
How are Smith & Nephew Medical, Ltd.’s devices classified under regulatory frameworks?
Smith & Nephew Medical, Ltd.’s devices are classified under three regulatory categories: Class I (generally low-risk devices with minimal regulatory controls), Class II (moderate-risk devices requiring special controls to ensure safety and effectiveness), and unclassified (U) devices, which may require additional evaluation or fall into niche categories. Classification depends on factors like intended use, risk level, and potential impact on patient safety, as determined by regulatory bodies like the FDA.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
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Catalogue (501)
Page 4 of 11| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Renasys Ab Drsg Kit W/Softport | 66021980 | FDA UDI | Class II | Active |
| Acticoat Flex7 6" X 6" | 66800427 | FDA UDI | U | Active |
| Allevyn Complete Care | 66807704 | FDA UDI | Class I | Active |
| Antimicrobial Gauze | 66801691 | FDA UDI | Class II | Active |
| Iv3000 12x9cm Carton Of 50 | 66004009 | FDA UDI | Class I | Active |
| Pico™ 7 | 66022024 | FDA UDI | Class II | Active |
| REPLICaRE 4X4IN (10X10CM) | 483100 | FDA UDI | Class I | Active |
| Renasys | 66020799 | FDA UDI | Class II | Active |
| SECURA No-Sting Barrier Film Wipes Bulk | 02676 | FDA UDI | Class I | Active |
| Allevyn | 66000663 | FDA UDI | Class I | Active |
| Acticoat 8"x16" | 20301 | FDA UDI | U | Active |
| Pico™ 7 | 66022011 | FDA UDI | Class II | Active |
| DURAFIBER Ag 20x30cm | 66800573 | FDA UDI | U | Active |
| Allevyn Ag Heel International | 66800098 | FDA UDI | U | Active |
| Leukostrip™ | 66002952 | FDA UDI | Class I | Active |
| Pico 14 | 66022042 | FDA UDI | Class II | Active |
| DURAFIBER Ag 2x45cm | 66800574 | FDA UDI | U | Active |
| NPWT Antimicrobial Large Gauze Roll | 66800391 | FDA UDI | Class II | Active |
| Allevyn Dressing 6x6" USA Ctn 10 | 66020093, 66000093 | FDA UDI | Class I | Active |
| ALLEVYN GENTLE 10CM x 10CM (4x4”)CTN 10 | 66802129 | FDA UDI | Class I | Active |
| Renasys | 66020797 | FDA UDI | Class II | Active |
| Pico 14 | 66022041 | FDA UDI | Class II | Active |
| Renasys Touch | 66020800 | FDA UDI | Class II | Active |
| Biobrane | 66027703 | FDA UDI | U | Active |
| Pico™ 7 | 66022007 | FDA UDI | Class II | Active |
| ALLEVYN Adhesive 3in x 3in | 66020400 | FDA UDI | Class I | Active |
| Viscopaste Pb7 3""x10yd Ctn 12 | 4956 | FDA UDI | U | Active |
| CicaCare 12cm x 6cm Ctn of 1 Global | 66250704 | FDA UDI | Class I | Active |
| Opsite Post Op 25x10cm Ctn 20 | 66000714 | FDA UDI | Class I | Active |
| ALLEVYN™ Ag+ | 66027663 | FDA UDI | U | Active |
| DURAMAX S Silicone super absorbent dressing | 66023135 | FDA UDI | Class I | Active |
| Pico | 66800955 | FDA UDI | Class II | Active |
| Renasys Go | 66021814 | FDA UDI | Class II | Active |
| Leukostrip™ | 66002953 | FDA UDI | Class I | Active |
| Allevyn Life Non-Brdr 10x20cm Ctn10 | 66801751 | FDA UDI | Class I | Active |
| Pico | 66800956 | FDA UDI | Class II | Active |
| Renasys Go | 66021815 | FDA UDI | Class II | Active |
| Exu-Dry Dressing 38x61cm Ctn 30 | 5999024 | FDA UDI | Class I | Active |
| Allevyn Sacrum Lge 22x22cm Ctn 10 | 66000451 | FDA UDI | Class I | Active |
| ALLEVYN™ Ag+ | 66027670 | FDA UDI | U | Active |
| Exu-Dry Lg Burn Jacket Pk 10 | 5999LJ1 | FDA UDI | Class I | Active |
| Pico | 66021360 | FDA UDI | Class II | Active |
| Durafiber 5x5 Ctn 10 | 66800559 | FDA UDI | Class I | Active |
| ALLEVYN™ Ag+ | 66027664 | FDA UDI | U | Active |
| Iv3000 6x8cm-Carton Of 100 | 4923 | FDA UDI | Class I | Active |
| Renasys Go | 66021739 | FDA UDI | Class II | Active |
| ALLEVYN Gentle Border Lite 5.5x12cm | 66800836 | FDA UDI | Class I | Active |
| Pico™ 7 | 66022028 | FDA UDI | Class II | Active |
| Ren/Asys Adhesive Gel Patch | 66801082 | FDA UDI | Class I | Active |
| VERSAJET III PRECISION Hydrosurgery System Hand Piece | 66802149 | FDA UDI | Class II | Active |
Related Companies
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FDA Recalls (3)
Recalls reported by this firm to the FDA. Listed at company level — FDA recall records don't identify a specific catalogue device.
Smith & Nephew Medical, Ltd. has three recall records initiated between March 11, 2024, and October 2, 2024. The records include one classified and one open status. The reasons cited involve battery depletion and recharge failures due to improper battery maintenance, as well as black particulate matter from carbon filter components potentially damaging NPWT pumps.
AI-generated summary of the recall records listed below. It describes what the records state and is not an assessment of this manufacturer.
| Date | Recall No. | Class | Status | Reason |
|---|---|---|---|---|
| Oct 2, 2024 | Z-0516-2025 | — | open, classified | Due to issues with battery depletion and inability to recharge if the batteries are not appropriately maintained. |
| Mar 11, 2024 | Z-1596-2024 | — | open, classified | Black particulate matter from the carbon filter component of the canisters entering the NPWT pump and potentially causing damage to the pump |
| Mar 11, 2024 | Z-1597-2024 | — | open, classified | Black particulate matter from the carbon filter component of the canisters entering the NPWT pump and potentially causing damage to the pump |
FDA Establishments (1)
Establishments registered with the FDA under this company group, matched by name.
- Smith & Nephew Medical Ltd HULL East Riding of Yorkshire · GB FEI 3002808194